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

Bromine → 6-Bromohexahydro-2h-3,5-methanocyclopenta[b]furan-2-one

HRID 75044
노트
인쇄 미리보기

반응식

HRID 75044 반응식
[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[CH:3]([C:8]([OH:10])=[O:9])[CH2:2]2.C([O-])(O)=O.[Na+].[Br:16]Br>O>[Br:16][CH:6]1[CH:5]2[O:9][C:8](=[O:10])[CH:3]3[CH2:2][CH:1]1[CH2:7][CH:4]23
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24408BromineHCID 789495-Norbornene-2-carboxylic acidHCID 516892Sodium Bicarbonate

생성물 1

HCID 2636406-Bromohexahydro-2h-3,5-methanocyclopenta[b]furan-2-one수율 67.7%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a solution of bicyclo[2.2.1]hept-5-ene-3-carboxylic acid (25.0 mL, 204.3 mmol) in NaHCO3 (51.5 g, 612.9 mmol) in water was added bromine (32.7 g, 204.3 mmol) dropwise at 0° C. The solution was stirred for 1 hour and extracted with ether, and the organic phase was washed successively with 1 N Na2S2SO3 solution and brine, and the organic phase was then dried (Na2SO4), filtered and concentrated in vacuo to afford 30 g of crude product that was used without further purification.

후처리

  1. extractionextracted with ether
  2. washthe organic phase was washed successively with 1 N Na2S2SO3 solution and brine
  3. dry with materialthe organic phase was then dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9793b01deecc420c961ee622a595885d
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829007B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트