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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 86635726, 화합물

HRID 1013336
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HRID 1013336 반응식
[Cl:1]N1C(=O)CCC1=O.[CH3:9][O:10][C:11]1[CH:12]=[C:13]([CH:17]=[CH:18][CH:19]=1)[CH:14]=[N:15][OH:16].O>CN(C=O)C>[Cl:1][C:13]1([CH:14]=[N:15][OH:16])[CH:17]=[CH:18][CH:19]=[C:11]([O:10][CH3:9])[CH2:12]1
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참가 물질

5

반응물 3

HCID 962WaterHCID 31398ChlorosuccinimideHCID 293577N-[(3-methoxyphenyl)methylidene]hydroxylamine

생성물 1

HCID 86635726HCID 86635726, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

N-chlorosuccinimide (32.2 g, 241 mmol) was added to a solution of 3-methoxybenzaldehyde oxime (30.4 g, 201 mmol) in DMF (200 ml) at RT, causing the temperature to rise briefly to 50° C. The reaction mixture was cooled in an ice bath, stirred overnight at RT, mixed with water (250 ml) while being cooled with ice and the precipitate formed was removed by suction-filtration. The filtrate was extracted with ether (3×400 ml) and the combined organic phases were washed with water (300 ml) and sat. aq. NaCl solution (300 ml), dried and the solvent was removed under vacuum. The desired product 1-chloro-1-hydroxyiminomethyl-3-methoxybenzene was obtained as a yellowish solid (32.86 g).

후처리

  1. customto rise briefly to 50° C
  2. temperatureThe reaction mixture was cooled in an ice bath
  3. temperaturewhile being cooled with ice
  4. customthe precipitate formed
  5. customwas removed by suction-filtration
  6. extractionThe filtrate was extracted with ether (3×400 ml)
  7. washthe combined organic phases were washed with water (300 ml) and sat. aq. NaCl solution (300 ml)
  8. customdried
  9. customthe solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-c495f19d278b49c9bbdfc663450aeb6a
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981883B2

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