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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → Diethyl 2-formylbenzylphosphonate thiosemicarbazone

HRID 1197747
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HRID 1197747 반응식
[CH:1]([C:3]1[CH:17]=[CH:16][CH:15]=[CH:14][C:4]=1[CH2:5][P:6](=[O:13])([O:10][CH2:11][CH3:12])[O:7][CH2:8][CH3:9])=O.[NH2:18][NH:19][C:20]([NH2:22])=[S:21].C(O)(=O)C>C(O)C>[CH:1](=[N:18][NH:19][C:20]([NH2:22])=[S:21])[C:3]1[CH:17]=[CH:16][CH:15]=[CH:14][C:4]=1[CH2:5][P:6](=[O:13])([O:10][CH2:11][CH3:12])[O:7][CH2:8][CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 2723789ThiosemicarbazideHCID 19104780Diethyl 2-formylbenzylphosphonate

생성물 1

HCID 53896642Diethyl 2-formylbenzylphosphonate thiosemicarbazone

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2.0 g (8 mmol) of the compound A and 0.73 g of thiosemicarbazide were dissolved or suspended in 200 ml of absolute ethanol. 2 ml of acetic acid were added and the mixture was boiled under reflux for 3 h. In the course of the slow cooling, the product D precipitated in crystalline form.

후처리

  1. temperatureunder reflux for 3 h
  2. customIn the course of the slow cooling, the product D precipitated in crystalline form

출처 및 근거

ORD 기록
ord-3b6b3d1703714625b1121304484cd5ea
출처 데이터셋
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05278152

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