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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 363738생성일: 2026년 10월 26일

Triethylamine → benzyl [(1S)-1-formyl-2-methylpropyl]carbamate

https://huagongshe.com/reaction/363738

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(S)-N-CBZ-valinolHCID 10900657—
용매Dimethyl SulfoxideHCID 679—
생성물benzyl [(1S)-1-formyl-2-methylpropyl]carbamateHCID 1100991585%

반응 단계

To a stirred solution of N-benzyloxycarbonyl-L-valinol (8.80 g, 0.037 mol) and triethylamine (30.00 g, 41.3 mL, 0.30 mol) in 100 mL dimethylsulfoxide under a nitrogen atmosphere was added a solution of sulfur trioxide pyridine complex (20.62 g, 0.130 mol) in dimethylsulfoxide (100 mL) dropwise via an addition funnel. An ice water bath was used to maintain the temperature of the reaction mixture below room temperature during the addition. After 30 min the cooling bath was removed and the reaction was allowed to warm to room temperature over 2 h. The brown solution was acidified with cold 2N HCl to approximately pH 2 and extracted with ether (3×150 mL). The combined organic layers were washed with brine, dried (anhydrous magnesium sulfate) and evaporated to give 7.40 g of N-benzyloxycarbonyl-L-valinal (84.8%) as a yellow oil. The resulting material can be used without purification or further purified using column chromatography (silica gel, 9:1 hexanes:ethyl acetate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05874585
출처 데이터셋uspto-grants-1999_02
ORD IDord-4183c2d4cc884544a594828553a7965d
출처 메모uspto-grants-1999_02