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2-(2-Bromophenoxymethyl)benzoic acid → 4-Bromo-6,11-dihydrodibenz[b,e]oxepin-11-one

HRID 1463180
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인쇄 미리보기

반응식

HRID 1463180 반응식
[Br:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[O:4][CH2:5][C:6]1[CH:14]=[CH:13][CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=O>FC(F)(F)C(OC(=O)C(F)(F)F)=O>[Br:1][C:2]1[C:3]2[O:4][CH2:5][C:6]3[CH:14]=[CH:13][CH:12]=[CH:11][C:7]=3[C:8](=[O:10])[C:15]=2[CH:16]=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 200859232-(2-Bromophenoxymethyl)benzoic acid

생성물 1

HCID 151138354-Bromo-6,11-dihydrodibenz[b,e]oxepin-11-one수율 53%

시약·촉매·용매 1

HCID 9845Trifluoroacetic anhydride촉매

실험 절차

A suspension of 2-(2-bromophenoxymethyl)benzoic acid (18.8 g, 0.06 mole) in 100 mL of trifluoracetic anhydride containing ten drops of boron trifluoride-ether complex was refluxed for four hours. The mixture was poured into ice water and then extracted with diethyl ether. Concentration of the ether solution under reduced pressure gave the pure product (9.2 g), mp 127°-130° C. pmr (CDCl3) δ: 7.28-8.19 (m, 76H, aromatic H); 6.99 (t, 1H, H2); 5.30 (s, 2H, ArCH2O).

후처리

  1. temperaturewas refluxed for four hours
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
extraction
extracted with diethyl ether

출처 및 근거

ORD 기록
ord-5ff624106fb04c18ad7c71f656c79638
출처 데이터셋
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05300282

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