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

Di-tert-butyl dicarbonate → HCID 22288417, 화합물

HRID 968243
노트
인쇄 미리보기

반응식

HRID 968243 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH2:9][OH:10])[CH:5]=[C:6]([CH3:8])[CH:7]=1.[O:11](C(OC(C)(C)C)=O)[C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=O>C(Cl)Cl>[OH:10][CH2:9][C:4]1[CH:3]=[C:2]([NH:1][C:12](=[O:11])[O:14][C:15]([CH3:18])([CH3:17])[CH3:16])[CH:7]=[C:6]([CH3:8])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 90495Di-tert-butyl dicarbonateHCID 15680639(3-Amino-5-methylphenyl)methanol

생성물 1

HCID 22288417HCID 22288417, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (3-amino-5-methylphenyl)methanol (1.0 g, 7.29 mmol) in CH2Cl2 (30 mL) was added BOC2O (1.75 g, 8.02 mmol) at room temperature. After 24 hours the mixture was concentrated. Flash column chromatography (30% EtOAc/hexanes) gave tert-butyl 3-(hydroxymethyl)-5-methylphenylcarbamate as a white solid. 1H-NMR (300 MHz, CDCl3) δ 7.20 (s, 1H), 7.18 (s, 1H), 6.85 (s, 1H), 6.45 (bs, 1H), 4.60 (s, 2H), 3.60 (bs, 2H), 2.32 (s, 3H), 1.50 (s, 9H).

후처리

  1. concentrationAfter 24 hours the mixture was concentrated

출처 및 근거

ORD 기록
ord-5f1ba161f00d4675b95c778570c57176
출처 데이터셋
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06958340B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트