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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Bromoanisole → HCID 18675130, 화합물

HRID 1635045
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HRID 1635045 반응식
Br[CH:2]1[C:7](=[O:8])[NH:6][C:5]2[CH:9]=[CH:10][CH:11]=[CH:12][C:4]=2[O:3]1.[Br:13][C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=1.[Sn](Cl)(Cl)(Cl)Cl>C(Cl)Cl>[Br:13][C:14]1[CH:15]=[CH:16][C:17]([O:20][CH3:21])=[C:18]([CH:2]2[C:7](=[O:8])[NH:6][C:5]3[CH:9]=[CH:10][CH:11]=[CH:12][C:4]=3[O:3]2)[CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 77304-BromoanisoleHCID 24287Tin tetrachloride2회HCID 18675343139115-80-3

생성물 1

HCID 18675130HCID 18675130, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To 2-bromo-2H-1,4-benzoxazin-3(4H)-one (I10) (1.40 g, 6.14 mmoles) in methylene chloride (20 mL) was added 4-bromoanisole and then tin (IV) chloride. Addition of tin (IV) chloride caused a brown solution to form. The solution was refluxed for 5 hours, diluted with methylene chloride (100 mL) and washed with water (2×50 mL). After drying over Magnesium sulphate the mixture was concentrated until the product (I11) precipitated (0.58 g). Concentration of the mother liquors and chromatography on silica gel afforded an additional amount of product (I11) (0.55 g).

후처리

  1. customto form
  2. temperatureThe solution was refluxed for 5 hours
  3. washwashed with water (2×50 mL)
  4. dry with materialAfter drying over Magnesium sulphate the mixture
  5. concentrationwas concentrated until the product (I11)
  6. customprecipitated (0.58 g)
  7. customConcentration of the mother liquors and chromatography on silica gel afforded an additional amount of product (I11) (0.55 g)

출처 및 근거

ORD 기록
ord-bdd861e6d9ee4df0bb98c360d37d65bd
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06509335B1

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