Methyl chloroformate → Ethyl 3-[3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphth-2-yl]propiolate

HRID 399283

반응식

HRID 399283 반응식
[CH3:1][C:2]1([CH3:21])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14]#[C:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:5]=[CH:4][C:3]1=2.[CH3:22]C1C(C#C)=CC2C(C)(C)CCC(C)(C)C=2C=1.COC(Cl)=O.C([Li])CCC>>[CH3:22][C:5]1[C:6]([C:14]#[C:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:7][C:8]2[C:9]([CH3:12])([CH3:13])[CH2:10][CH2:11][C:2]([CH3:21])([CH3:1])[C:3]=2[CH:4]=1

참가 물질

5

실험 절차

Employing the same general procedure as used for the preparation of ethyl 3-[5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl]propiolate (Compound A), but instead using 1.9 g of (3-methyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)ethyne, 940 mgs (10 mmols) of methylchloroformate and 8.8 mmols of n-butyllithium the title compound was obtained as an oil.

출처 및 근거

ORD 기록
ord-aa3cf2f56d264cf5b433a763c72ea803
출처 데이터셋
uspto-grants-1998_10
특허 번호
US05817836

연결된 노트

불러오는 중…