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

Benzyl Bromide → HCID 59403479, 화합물

HRID 1514194
노트
인쇄 미리보기

반응식

HRID 1514194 반응식
[OH:1][C:2]1[CH:13]=[CH:12][C:5]2[C:6](=[O:11])[NH:7][CH2:8][CH2:9][O:10][C:4]=2[CH:3]=1.[CH2:14](Br)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C.CCOC(C)=O.O>[C:15]1([CH2:14][O:1][C:2]2[CH:13]=[CH:12][C:5]3[C:6](=[O:11])[NH:7][CH2:8][CH2:9][O:10][C:4]=3[CH:3]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 59403478HCID 59403478, 화합물

생성물 1

HCID 59403479HCID 59403479, 화합물수율 64.5%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 22728543Water ethylacetate용매

반응 조건

온도
60 °C

실험 절차

A mixture of 8-hydroxy-3,4-dihydro-1,4-benzoxazepin-5(2H)-one (Preparation 26) (8.66 g, 48.3 mmol), benzyl bromide (6.32 ml, 53.2 mmol) and potassium carbonate (20.04 g, 145 mmol) in DMF (80 ml) was stirred and heated at 60° C. for 2 hours. The cooled reaction was diluted with EtOAc/water (300 ml of each) and the aqueous extracted with EtOAc (2×75 ml). Combined organics were washed with 3×100 ml of water, dried (magnesium sulphate), evaporated, triturated with ether and filtered off to give the title compound (8.39 g) as a white solid. MS (ES) C16H15NO3 requires 269; found 270 [M+H]+.

후처리

  1. customThe cooled reaction
  2. extractionaqueous extracted with EtOAc (2×75 ml)
  3. washCombined organics were washed with 3×100 ml of water
  4. dry with materialdried (magnesium sulphate)
  5. customevaporated
  6. customtriturated with ether
  7. filtrationfiltered off

출처 및 근거

ORD 기록
ord-6d70ed0ce0d54547afd7bd62edeb6c19
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08222245B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트