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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44143생성일: 2026년 10월 24일

[(S)-1-(Methoxy-methyl-carbamoyl)-2-methyl-propyl]carbamic acid benzyl ester → benzyl [(1S)-1-formyl-2-methylpropyl]carbamate

https://huagongshe.com/ko/reaction/44143

반응식

참여 물질

역할이름HCID투입량
반응물[(S)-1-(Methoxy-methyl-carbamoyl)-2-methyl-propyl]carbamic acid benzyl esterHCID 10469699—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물benzyl [(1S)-1-formyl-2-methylpropyl]carbamateHCID 1100991599.8%

반응 조건

온도0 °C

반응 단계

To a solution of [(S)-1-(Methoxy-methyl-carbamoyl)-2-methyl-propyl]-carbamic acid benzyl ester (8) (33 g, 112 mmol) in dry THF (300 mL) at −30 to −40° C. was added LiAlH4 (4.3 g, 113 mmol) portion wise over a period of 45 min. The reaction mixture was warmed to 0° C. and stirred at this temperature for 2 h. The reaction mixture was quenched with 1 M KHSO4 (330 mL) at 0° C. then 10% w/v Rochelle's salt (aq) (330 mL) was added and the mixture stirred for 20 minutes, then extracted with EtOAc (2×700 mL). The combined organic phases were washed with 10% w/v Rochelle's salt (aq) (330 mL) and brine (450 mL), dried over MgSO4, filtered and concentrated under vacuum to obtain the desired aldehyde as a clear oil (26.3 g) (AnalpH2_MeOH—4 min) Rt 2.59 min; m/z 236 (MH)+. (This was used without further purification in the next step.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541363B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d933afcd3a1b4cc296a607e24d0d3a68
출처 메모uspto-grants-2013_09