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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Benzenepropanoic acid → beta-Bromobenzenepropanoic acid

HRID 66923
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인쇄 미리보기

반응식

HRID 66923 반응식
[C:1]([OH:11])(=[O:10])[CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Br:12]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.C1(=O)NC(=O)CC1>C(Cl)(Cl)(Cl)Cl.O>[Br:12][CH:3]([C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1)[CH2:2][C:1]([OH:11])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 107Benzenepropanoic acidHCID 7187Benzoyl PeroxideHCID 11439SuccinimideHCID 67184N-bromobutanimide

생성물 1

HCID 226117beta-Bromobenzenepropanoic acid

시약·촉매·용매 2

HCID 962Water용매
HCID 5943
Carbon Tetrachloride
용매

실험 절차

A mixture of 100 g (0.667 mol) of hydrocinnamic acid, 120 g (0.674 mol) of N-bromosuccinimide, and 1.8 g of benzoyl peroxide (BPO) in 900 ml of CCl4 was heated at reflux for 20 hr under nitrogen. After cooling to room temperature the reaction mixture was filtered. The filtrate when stripped to dryness yielded only a small amount of additional material which was combined with the original solid and the whole was slurried for 2 hr with warm water to dissolve the succinimide. The slurry was filtered and rinsed with water again and oven dried at 50° C. overnight to 120.8 g (79%) of material which is pure enough for the next step. Material recrystallized from toluene melts 138.5°-140.0° C.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 20 hr under nitrogen
  3. filtrationwas filtered
  4. customyielded only a small amount of additional material which
  5. filtrationThe slurry was filtered
  6. washrinsed with water again
  7. dry with materialoven dried at 50° C. overnight to 120.8 g (79%) of material which
  8. customMaterial recrystallized from toluene melts 138.5°-140.0° C.

출처 및 근거

ORD 기록
ord-02d0e14e6e874c8f85ccd141d69a175e
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04343893

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