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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1903생성일: 2026년 10월 23일

Benzyl Alcohol → Methyl 3-(((benzyloxy)carbonyl)amino)-3-methylbutanoate

https://huagongshe.com/ko/reaction/1903

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물4-Methoxy-2,2-dimethyl-4-oxobutanoic acidHCID 12602176—
용매BenzeneHCID 241—
생성물Methyl 3-(((benzyloxy)carbonyl)amino)-3-methylbutanoateHCID 1504255475.1%

반응 단계

To 14.7 g (91.8 mmol) of 2,2-dimethylbutanedioic acid-4-methyl ester in 150 mL of benzene was added 13 mL of triethylamine (9.4 g, 93 mmol) followed by 21.8 mL of diphenylphosphoryl azide (27.8 g, 101 mmol). The mixture was heated under nitrogen at reflux for 45 minutes then 19 mL (19.9 g, 184 mmol) of benzyl alcohol was added and refluxing continued for 16 hours. The mixture was cooled, filtered and the filtrate concentrated to a minimum volume under vacuum. The residue was redissolved in 250 mL of ethyl acetate, washed with water, saturated aqueous sodium bicarbonate (2×) and brine. The organic layer was removed, dried over magnesium sulfate, filtered and the filtrate concentrated to a minimum volume under vacuum. The crude product was purified by medium pressure liquid chromatography on silica, eluting with hexane/ethyl acetate (4:1), to afford 18.27 g (68.9 mmol, 75%) of the product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726319
출처 데이터셋uspto-grants-1998_03
ORD IDord-4b176a6bf0704d8d9641aa04cf712b48
출처 메모uspto-grants-1998_03