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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Prop-2-en-1-yl 3-nitrobenzoate → Allyl 3-aminobenzoate

HRID 2072334
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HRID 2072334 반응식
[CH2:1]([O:4][C:5](=[O:15])[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-])=O)[CH:7]=1)[CH:2]=[CH2:3]>CO.[Co]=S>[CH2:1]([O:4][C:5](=[O:15])[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([NH2:12])[CH:7]=1)[CH:2]=[CH2:3]
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참가 물질

4

반응물 1

HCID 14980143Prop-2-en-1-yl 3-nitrobenzoate

생성물 1

HCID 18930599Allyl 3-aminobenzoate수율 89.5%

시약·촉매·용매 2

HCID 14832Cobalt sulfide촉매HCID 887Methanol용매

실험 절차

478 g of 3-nitrobenzoic acid allyl ester are hydrogenated in 2 l of methanol at 110° C and 30-50 bars of H2 in the presence of 60 g of a cobalt sulphide paste which contains 30% of CoS3. The absorption of H2 has ceased in 2 hours. After cooling, 30 g of NaHCO3 are added to the methanol solution which contains the suspended catalyst and the mixture is stirred for 10 minutes and filtered. Distillation gives 366 g of 3-aminobenzoic acid allyl ester, boiling point 0.35 = 135° C; ND20 = 1.5657.

후처리

  1. customThe absorption of H2
  2. temperatureAfter cooling
  3. addition30 g of NaHCO3 are added to the methanol solution which
  4. filtrationfiltered
  5. distillationDistillation

출처 및 근거

ORD 기록
ord-da97bd8c040e4620a87a73af3fc81776
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04051177

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