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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Boron tribromide → Phenol, 2-amino-4-(methylsulfonyl)-

HRID 1644385
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HRID 1644385 반응식
C[O:2][C:3]1[CH:9]=[CH:8][C:7]([S:10]([CH3:13])(=[O:12])=[O:11])=[CH:6][C:4]=1[NH2:5].B(Br)(Br)Br>C(Cl)(Cl)Cl>[CH3:13][S:10]([C:7]1[CH:8]=[CH:9][C:3]([OH:2])=[C:4]([NH2:5])[CH:6]=1)(=[O:11])=[O:12]
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 27595925-Methanesulfonyl-2-methoxyaniline

생성물 1

HCID 7382Phenol, 2-amino-4-(methylsulfonyl)-

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

The title compound was prepared by reacting 2-methoxy-5-methylsulfonyl aniline (5.0 g, 24.8 mmol) with boron tribromide (26 mmol, 26 mL, 1M in dichloromethane) in chloroform (30 m L) at 0° C. After 20 minutes, the reaction was quenched with sodium bicarbonate and the ph of the aqueous phase was adjusted to pH 7 and extracted with ethyl acetate. Concentration under reduced pressure gave 690 mg of product as an orange solid (15%).

후처리

  1. customat 0° C
  2. customthe reaction was quenched with sodium bicarbonate
  3. extractionextracted with ethyl acetate
  4. concentrationConcentration under reduced pressure

출처 및 근거

ORD 기록
ord-76bc956b94ce4f85a0a5df5a37e12503
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08124602B2

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