2-Dimethylaminopyridine → (Trimethylsilyl)ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate

HRID 233108

반응식

HRID 233108 반응식
[CH3:1][C:2]1([CH3:24])[C:11]2[CH:10]=[C:9]([C:12]#[C:13][C:14]3[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[CH:16][CH:15]=3)[CH:8]=[CH:7][C:6]=2[C:5](=[O:23])[CH2:4][CH2:3]1.CN(C1C=CC=CN=1)C.[CH3:34][Si:35]([CH:38](O)[CH3:39])([CH3:37])[CH3:36].Cl.CN(C)CCCN=C=NCC>C(Cl)Cl>[CH3:1][C:2]1([CH3:24])[C:11]2[CH:10]=[C:9]([C:12]#[C:13][C:14]3[CH:15]=[CH:16][C:17]([C:18]([O:20][CH2:39][CH2:38][Si:35]([CH3:37])([CH3:36])[CH3:34])=[O:19])=[CH:21][CH:22]=3)[CH:8]=[CH:7][C:6]=2[C:5](=[O:23])[CH2:4][CH2:3]1

참가 물질

6

반응 조건

온도
25 °C

실험 절차

To a solution of 0.24 g (0.73 mmol) of 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoic acid (Compound 7) in 10 ml of dry CH2Cl2 was added 0.09 g (0.74 mmol) of dimethylaminopyridine, 0.115 ml (0.80 mmol) of trimethylsilylethanol and 0.17 g (0.88 mmol) of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride. The reaction mixture was stirred at 25° C. for 5 hours, washed with sat. aqueous NaHCO3 and brine, dried over Na2SO4 and concentrated in vacuo to an oil. Purification by flash chromatography (silica, 10% EtOAc-hexane) yielded the title compound as a white solid.

후처리

  1. washwashed with sat. aqueous NaHCO3 and brine
  2. dry with materialdried over Na2SO4
  3. concentrationconcentrated in vacuo to an oil
  4. customPurification by flash chromatography (silica, 10% EtOAc-hexane)

출처 및 근거

ORD 기록
ord-0007a111eb0447c487d465fd0429d3bc
출처 데이터셋
uspto-grants-1997_01
특허 번호
US05591858

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