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2-Chlorobenzaldehyde → HCID 11587130、化合物

HRID 2235267
ノート
印刷プレビュー

反応式

HRID 2235267 の反応式
[CH:1]1([N:7]2[CH:11]([CH3:12])[CH2:10][CH2:9][C:8]2=[O:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Li+].CC([N-]C(C)C)C.Cl[C:23]1[CH:30]=[CH:29][CH:28]=[CH:27][C:24]=1[CH:25]=O.[Cl-].[NH4+].C(N(CC)CC)C.CS(Cl)(=O)=O.C1CCN2C(=NCCC2)CC1>C1COCC1.O>[CH2:25]([CH:9]1[CH2:10][CH:11]([CH3:12])[N:7]([CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[C:8]1=[O:13])[C:24]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:23]=1
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

10

反応物 7

HCID 69962-ChlorobenzaldehydeHCID 8471TriethylamineHCID 25517Ammonium ChlorideHCID 31297Methanesulfonyl chlorideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 2724682Lithium diisopropylamideHCID 103523081-Cyclohexyl-5-methyl-pyrrolidin-2-one

生成物

1
HCID 11587130HCID 11587130、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

Charge a flask with 1-cyclohexyl-5-methyl-pyrrolidin-2-one (U.S. Pat. No. 6,743,819, 500 mg, 2.8 mmol), dissolve in THF (30 mL) and cool to −78° C. under nitrogen. Add LDA (2M, 1.7 mL, 3.3 mmol) and stir at −78° C. for 10 minutes. Add 2-chlorobenzaldehyde (500 mg, 3.6 mmol) and warm to room temperature. Pour into saturated aqueous ammonium chloride and extract with methylene chloride. Dry over sodium sulfate, filter and concentrate. Dissolve the residue in THF (30 mL) and add triethylamine (360 mg, 3.6 mmol) and methanesulfonyl chloride (380 mg, 3.3 mmol). Stir at room temperature for 2 hours and filter. Add DBU (440 mg, 3.6 mmol) to the filtrate and stir overnight. Pour the reaction into water and extract with methylene chloride. Dry over sodium sulfate, filter and concentrate. Purify residue over silica gel (5:1 hexanes:ethyl acetate). Dissolve the residue in methanol (10 mL) and add 10% palladium on carbon (40 mg) and stir under a balloon of hydrogen for 3 days. Filter through celite® and concentrate. Purify over silica gel (9:1 hexanes:ethyl acetate) to afford two separable isomers.

後処理

  1. extractionextract with methylene chloride
  2. dry with materialDry over sodium sulfate
  3. filtrationfilter
  4. concentrationconcentrate
  5. dissolutionDissolve the residue in THF (30 mL)
  6. filtrationfilter
  7. additionPour
  8. extractionextract with methylene chloride
  9. dry with materialDry over sodium sulfate
  10. filtrationfilter
  11. concentrationconcentrate
  12. dissolutionDissolve the residue in methanol (10 mL)
  13. additionadd 10% palladium on carbon (40 mg)
  14. stirringstir under a balloon of hydrogen for 3 days
  15. filtrationFilter through celite®
  16. concentrationconcentrate
  17. customPurify over silica gel (9:1 hexanes:ethyl acetate)
  18. customto afford two separable isomers

出典と根拠

ORDレコード
ord-ca4c7873b97a4339a3165b64e97609da
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07713979B2

反応ノート

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