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Diisopropylamine → (1R,5R,6R)-6-fluoro-bicyclo[3.1.0]hex-2-ene-2,6-dicarboxylic acid 2-benzyl ester 6-ethyl ester

HRID 1835568
ノート
印刷プレビュー

反応式

HRID 1835568 の反応式
[CH2:1]([Li])[CH2:2][CH2:3]C.C(N[CH:10]([CH3:12])[CH3:11])(C)C.[F:13][C@@:14]1([C:21]([O:23][CH2:24][CH3:25])=[O:22])[C@@H:19]2[C@H:15]1[CH2:16][CH2:17][C:18]2=O.C1C=CC(N(S(C(F)(F)F)(=O)=O)S(C(F)(F)F)(=O)=[O:34])=CC=1.[O:47]1[CH2:51]CC[CH2:48]1>CCCCCC>[CH2:24]([O:23][C:21]([C@:14]1([F:13])[C@@H:19]2[C@H:15]1[CH2:16][CH:17]=[C:18]2[C:48]([O:47][CH2:51][C:11]1[CH:10]=[CH:12][CH:3]=[CH:2][CH:1]=1)=[O:34])=[O:22])[CH3:25]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 7912DiisopropylamineHCID 8028Tetrahydrofuran3 回HCID 142176Phenyl triflimideHCID 10607583HCID 10607583、化合物HCID 178418339Butyllithium

生成物 1

HCID 11738241(1R,5R,6R)-6-fluoro-bicyclo[3.1.0]hex-2-ene-2,6-dicarboxylic acid 2-benzyl ester 6-ethyl ester

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

反応条件

温度
0 °C

実験手順

A 2.47 M hexane solution of butyl lithium in an amount of 28.8 mL was added to a solution of 7.83 g of diisopropylamine dissolved in 84 mL of tetrahydrofuran, which was cooled to 0° C. The solution was stirred for 15 minutes, followed by cooling to −62° C. Subsequently, a solution of 12.0 g of ethyl (1R,5R,6R)-6-fluoro-2-oxo-bicyclo[3.1.0]hexane-6-carboxylate dissolved in 40 mL of tetrahydrofuran was added dropwise thereto, while being maintained at −62 to −58° C. One hour later, a solution of 25.3 g of N-phenyl-bis(trifluoromethanesulfonimide) dissolved in 84 mL of tetrahydrofuran was added dropwise thereto over 15 minutes, while maintained at −62 to −60° C. The reaction solution was allowed to naturally warm to room temperature, and was further stirred for one hour. The reaction was quenched with a saturated aqueous solution of sodium hydrogencarbonate, followed by extraction with diethyl ether. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, and was subsequently dried over anhydrous magnesium sulfate. After the desiccant was filtered off, the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel: Wako gel C200 (produced by Wako Pure Chemical Industries Ltd.), eluent: hexane-ethyl acetate=20:1). Immediately, the produced ethyl (1R,5R,6R)-6-fluoro-2-trifluoromethanesulfonyloxy-bicyclo[3.1.0]hex-2-ene-6-carboxylate was dissolved in 195 mL of N,N-dimethylformamide, and 389 mg of palladium acetate, 910 mg of triphenylphosphine, and 12.5 g of benzyl alcohol were added thereto, followed by addition of 11.7 g of triethylamine. Subsequently, the mixture was stirred under a carbon monoxide atmosphere for 4.5 hours at room temperature. 1M hydrochloric acid was added to the reaction mixture, followed by extractions with diethyl ether twice. The organic layers were combined, and the combined organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate and a saturated aqueous solution of sodium chloride, followed by drying over anhydrous magnesium sulfate. After the desiccant was filtered off, the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel: Wako gel C200 (produced by Wako Pure Chemical Industries Ltd.), eluent: hexane-ethyl acetate=10:1 to 1:1), thereby yielding 6.42 g of (1R,5R,6R)-6-fluoro-bicyclo[3.1.0]hex-2-ene-2,6-dicarboxylic acid 2-benzyl ester 6-ethyl ester.

後処理

  1. temperatureby cooling to −62° C
  2. additionwas added dropwise
  3. temperaturewhile being maintained at −62 to −58° C
  4. additionwas added dropwise
  5. waitover 15 minutes
  6. temperaturewhile maintained at −62 to −60° C
  7. temperatureto naturally warm to room temperature
  8. stirringwas further stirred for one hour
  9. customThe reaction was quenched with a saturated aqueous solution of sodium hydrogencarbonate
  10. extractionfollowed by extraction with diethyl ether
  11. washThe organic layer was washed with water
  12. dry with materiala saturated aqueous solution of sodium chloride, and was subsequently dried over anhydrous magnesium sulfate
  13. filtrationAfter the desiccant was filtered off
  14. concentrationthe filtrate was concentrated under reduced pressure
  15. customThe residue was purified by column chromatography (silica gel: Wako gel C200 (produced by Wako Pure Chemical Industries Ltd.), eluent: hexane-ethyl acetate=20:1)
  16. dissolutionImmediately, the produced ethyl (1R,5R,6R)-6-fluoro-2-trifluoromethanesulfonyloxy-bicyclo[3.1.0]hex-2-ene-6-carboxylate was dissolved in 195 mL of N,N-dimethylformamide
  17. addition389 mg of palladium acetate, 910 mg of triphenylphosphine, and 12.5 g of benzyl alcohol were added
  18. additionfollowed by addition of 11.7 g of triethylamine
  19. stirringSubsequently, the mixture was stirred under a carbon monoxide atmosphere for 4.5 hours at room temperature
  20. addition1M hydrochloric acid was added to the reaction mixture
  21. extractionfollowed by extractions with diethyl ether twice
  22. washthe combined organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate
  23. dry with materialby drying over anhydrous magnesium sulfate
  24. filtrationAfter the desiccant was filtered off
  25. concentrationthe filtrate was concentrated under reduced pressure
  26. customThe residue was purified by column chromatography (silica gel: Wako gel C200 (produced by Wako Pure Chemical Industries Ltd.), eluent: hexane-ethyl acetate=10:1 to 1:1)

出典と根拠

ORDレコード
ord-ac784d8fa089433393f38e9167155fd9
出典データセット
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06770676B2

反応ノート

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