홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

HCID 178501239, 화합물 → HCID 178453956, 화합물

HRID 928233
노트
인쇄 미리보기

반응식

HRID 928233 반응식
[C:1]([O:5][C:6]([NH:8][C@H:9]1[CH2:14][CH2:13][C@H:12]([C:15](OC)=[O:16])[CH2:11][CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>C1COCC1>[OH:16][CH2:15][C@H:12]1[CH2:11][CH2:10][C@H:9]([NH:8][C:6](=[O:7])[O:5][C:1]([CH3:3])([CH3:2])[CH3:4])[CH2:14][CH2:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178501239HCID 178501239, 화합물

생성물 1

HCID 178453956HCID 178453956, 화합물수율 69%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of trans-methyl 4-(tert-butoxycarbonylamino)cyclohexanecarboxylate (9.0 g, 35 mmol) in THF (70 mL) was added slowly a 2.0 M solution of LiAH4 in THF (20 mL, mmol) at −78° C. The reaction was warmed slowly to room temperature (over 4 h), and quenched by dropwise addition of water (5 mL), followed by addition of NaOH (5 mL) and Na2SO4. The mixture was stirred for 20 min and filtered. The filtrate was dried (Na2SO4), and concentrated. The crude mixture was purified by Isco to provide tert-butyl trans-4-(hydroxymethyl)cyclohexylcarbamate (5.5 g, 69%) as a white solid.

후처리

  1. customquenched by dropwise addition of water (5 mL)
  • additionfollowed by addition of NaOH (5 mL) and Na2SO4
  • filtrationfiltered
  • dry with materialThe filtrate was dried (Na2SO4)
  • concentrationconcentrated
  • customThe crude mixture was purified by Isco
  • 출처 및 근거

    ORD 기록
    ord-e254e2e0ac8c41e4b5db3696e7fcd561
    출처 데이터셋
    uspto-grants-2016_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09290499B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트