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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1906생성일: 2026년 10월 23일

Benzyl Alcohol → Boc-DTrp-OBzl

https://huagongshe.com/ko/reaction/1906

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물WaterHCID 962—
반응물N-((tert-Butoxy)carbonyl)-D-tryptophanHCID 111050—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물Boc-DTrp-OBzlHCID 10739405—

반응 단계

Finely divided t-butoxycarbonyl-D-tryptophan (3 g, 10 mmol) was suspended in methylene chloride and benzyl alcohol (1.08 mL, 10 mmol) and 4-dimethylaminopyridine (0.12 g, 1 mmol) were added and stirred at room temperature. Solid 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.92 g, 10 mmol) was then added in three roughly equal portions over 5 minutes. The reaction mixture was stirred for 3 hours at room temperature during which time the reaction mixture became a homogeneous solution. The reaction mixture was poured into water (100 mL) and extracted with methylene chloride (2×50 mL). The combined methylene chloride layers were washed with 5% aqueous citric acid solution (100 mL) and 5% aqueous sodium bicarbonate solution (100 mL). The resulting methylene chloride layer was dried over magnesium sulfate, filtered and evaporated under vaccum to give an off-white solid. This solid material was chromatographed on silica gel using ethyl acetate/hexanes (2:3 v/v) as eluant. This afforded 3.56 g (91%) of the desired benzyl ester as a white amorphous powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726319
출처 데이터셋uspto-grants-1998_03
ORD IDord-8d15441bff9244cf8bac899003f74801
출처 메모uspto-grants-1998_03