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Boron tribromide → HCID 178524229, 화합물

HRID 719176
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HRID 719176 반응식
C[O:2][C:3]1[C:8]2=[CH:9][CH:10]=[C:11]3[C:20]([N:19]=[C:18]4[C:13]([CH:14]=[CH:15][CH:16]=[C:17]4[C:21]([OH:23])=[O:22])=[N:12]3)=[C:7]2[CH:6]=[CH:5][CH:4]=1.B(Br)(Br)Br>ClCCl>[OH:2][C:3]1[C:8]2=[CH:9][CH:10]=[C:11]3[C:20]([N:19]=[C:18]4[C:13]([CH:14]=[CH:15][CH:16]=[C:17]4[C:21]([OH:23])=[O:22])=[N:12]3)=[C:7]2[CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 111202464-Methoxy-benzo[a]phenazine-11-carboxylic Acid

생성물 1

HCID 178524229HCID 178524229, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 4-methoxy-benzo[a]phenazine-11-carboxylic acid (II.1, see Reference Example 1A) (441 mg) in dichloromethane (30 mL) cooled to 0° C. was added a 1.0M solution of boron tribromide in dichloromethane (7.25 mL). The reaction mixture was allowed to warm to room temperature and then stirred for 16 hours. The mixture was then poured onto ice/water yielding 4-hydroxy-benzo[a]phenazine-11-carboxylic acid as a red/brown solid which was collected by filtration and air dried (230 mg).

후처리

  1. additionThe mixture was then poured onto ice/water

출처 및 근거

ORD 기록
ord-72cb2f6bc7fd4aacaae544f1f0850805
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07132419B2

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