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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 970784생성일: 2026년 10월 24일

Methyl (R)-(+)-2-isocyanato-3-phenylpropionate → (R)-2-(4-Phenoxymethyl-benzyloxycarbonylamino)-3-phenyl-propionic Acid Methyl Ester

https://huagongshe.com/ko/reaction/970784

반응식

참여 물질

역할이름HCID투입량
반응물Methyl (R)-(+)-2-isocyanato-3-phenylpropionateHCID 6558897—
반응물(4-(Phenoxymethyl)phenyl)methanolHCID 11333367—
촉매4-(Dimethylamino)pyridineHCID 14284—
생성물(R)-2-(4-Phenoxymethyl-benzyloxycarbonylamino)-3-phenyl-propionic Acid Methyl EsterHCID 1299090495.4%

반응 단계

(R)-Phenylalanine methyl ester hydrochloride (6.5 g, 30 mmol) was dissolved in methylene chloride and cooled to 0C. Phosgene (2M in toluene, 21.0 ml, 42.0 mmol) was added followed by pyridine (9.0 ml, 111 mmol). The mixture was allowed to warm to room temperature and was stirred for three hours. The mixture was then poured into dilute HCl. The layers were separated. The organic extracts were washed, dried, and concentrated to give about 5.8 g of a clear oil of (R)-2-isocyanato-3-phenyl-propionic acid methyl ester 5. 4-Phenoxymethylphenylmethanol 4 (0.857 g, 4.0 mmol), (R)-2-isocyanato-3-phenyl-propionic acid methyl ester 5 (1.026 g, 5.0 mmol) and 4-dimethylaminopyridine (DMAP) (10 mg) were combined, heated until molten, and stirred for 20 min. Upon cooling, the residue was purified by chromatography to give about 1.6 g of (R)-2-(4-phenoxymethyl-benzyloxycarbonylamino)-3-phenyl-propionic acid methyl ester 6.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07312230B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-0e6a776da3e0497d8c294e4f32ebdb61
출처 메모uspto-grants-2007_12