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2-Naphthoyl chloride → HCID 21932517、化合物

HRID 634582
ノート
印刷プレビュー

反応式

HRID 634582 の反応式
C([N-]C(C)C)(C)C.[Li+].[C:9]([O:12][C:13]([CH3:22])([CH2:15][CH2:16][CH2:17][CH:18]([CH3:21])[CH:19]=[CH2:20])[CH3:14])(=[O:11])[CH3:10].[CH:23]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH:26]=[CH:25][C:24]=1[C:33](Cl)=[O:34]>C1COCC1>[CH:23]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH:26]=[CH:25][C:24]=1[C:33](=[O:34])[CH2:10][C:9]([O:12][C:13]([CH3:22])([CH2:15][CH2:16][CH2:17][CH:18]([CH3:21])[CH:19]=[CH2:20])[CH3:14])=[O:11]
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

5

反応物 3

HCID 752462-Naphthoyl chlorideHCID 1038262,6-Dimethyl-7-octen-2-yl acetateHCID 2724682Lithium diisopropylamide

生成物 1

HCID 21932517HCID 21932517、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

Lithium diisopropylamide in the amount of (100.0 mL of a 2.0 M solution, 0.201 mol) is placed into a 500 mL three-necked round-bottomed flask fitted with a magnetic stirrer, internal thermometer, argon inlet, and addition ftnnel. The flask is cooled to −78° C. 2,6-Dimethyl-7-octen-2-yl acetate in the amount of (18.75 g, 0.095 mol) is dissolved in THF (5 mL) and the resulting solution added to the flask over 45 min. Once addition is complete, the mixture is stirred for an additional 15 min before being treated with a solution of 2-naphthoyl chloride in the amount of (17.00 g, 0.089 mol) dissolved in THF (25 mL) over 30 min. The mixture is warmed to −20° C. and stirred at that temperature for 18 h. After warming to 0° C., the mixture is quenched with 20% HCl (55 mL). The mixture is poured into a separatory funnel containing ether (150 mL) and water (250 mL). The aqueous layer is extracted with ether (150 mL). The combined organic layers are washed with saturated NaHCO3 solution (2×100 mL), water (2×150 mL) and brine (150 mL), dried over MgSO4 and filtered. The solvent is removed by rotary evaporation to give an orange/red oil. The oil is purified by column chromatography (elution with 2% ethyl acetate dissolved in petrolewn ether) to give an oil. Purity of the product is determined by thin layer chromatography and the structure confirmed by 1H and 13C NMR.

後処理

  1. customfitted with a magnetic stirrer
  2. additioninternal thermometer, argon inlet, and addition ftnnel
  3. additionthe resulting solution added to the flask over 45 min
  4. additionOnce addition
  5. temperatureThe mixture is warmed to −20° C.
  6. stirringstirred at that temperature for 18 h
  7. temperatureAfter warming to 0° C.
  8. customthe mixture is quenched with 20% HCl (55 mL)
  9. additionThe mixture is poured into a separatory funnel
  10. additioncontaining ether (150 mL) and water (250 mL)
  11. extractionThe aqueous layer is extracted with ether (150 mL)
  12. washThe combined organic layers are washed with saturated NaHCO3 solution (2×100 mL), water (2×150 mL) and brine (150 mL)
  13. dry with materialdried over MgSO4
  14. filtrationfiltered
  15. customThe solvent is removed by rotary evaporation
  16. customto give an orange/red oil
  17. customThe oil is purified by column chromatography (elution with 2% ethyl acetate dissolved in petrolewn ether)
  18. customto give an oil

出典と根拠

ORDレコード
ord-812481fcdb744b78b80760dff176f6ef
出典データセット
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06184188B2

反応ノート

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