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HRID 258235생성일: 2026년 10월 25일

Diazald → Methyl deoxycholate

https://huagongshe.com/reaction/258235

반응식

참여 물질

역할이름HCID투입량
반응물DiazaldHCID 6628—
반응물DiazomethaneHCID 9550—
반응물Deoxycholic AcidHCID 222528—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Methyl deoxycholateHCID 229346—

반응 단계

Deoxycholic acid (0.54 g, 1.4 mmol) in THF (10 ml) at 0° C. was treated dropwise with freshly prepared diazomethane in ether (prepared in the usual manner from diazald) until the yellow colour persisted. After 15 minutes at 0° C. the solvent was evaporated to yield a white foam (0.60 g). The compound would not recrystallise, although gas chromatography showed the product to be 99% pure. The product was further purified by preparative silica tlc. (solvent system: EtOAc/CH2Cl2 /AcOH--10:10:1) to afford pure methyl deoxycholate2 (0.45 g, 80%) as a foam: 1H NMR (60 MHz; CDCl3) δ0.67 (3H, s, 18-CH3), 0.92 (3H, s, 18-CH3), 2.18 (2H, s [exchanges on adding D2O], 3α and 12α OH's), 3.2-3.7 (1H, m. 3β-H), 3.65 (3 H, s, --OMe), 3.8-4-1 (1H, m, 12β-H); IR (nujol mull) 3368 (OH's), 1740 (C=O) cm-1 ; MS: Found m/z 388.2951; C25H40O3 (M-H2O) requires 388.2977.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05266566
출처 데이터셋uspto-grants-1993_11
ORD IDord-b0c15b2254654d1e958362c00ec2584b
출처 메모uspto-grants-1993_11