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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cyanamide → HCID 86643043, 화합물

HRID 2192202
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HRID 2192202 반응식
[N:1]#[C:2][NH2:3].C[O-].[Na+:6].C(O[C:10](=[C:13]([C:16]#[N:17])[C:14]#[N:15])[CH2:11][CH3:12])C>C(O)C>[C:2]([N-:3][C:10](=[C:13]([C:16]#[N:17])[C:14]#[N:15])[CH2:11][CH3:12])#[N:1].[Na+:6]
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참가 물질

5

반응물 3

HCID 9864CyanamideHCID 2314702-(1-Ethoxypropylidene)malononitrileHCID 10942334Sodium Methoxide

생성물 1

HCID 86643043HCID 86643043, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
25 °C

실험 절차

In portions, 7.56 g of cyanamide are added to a solution of 32.38 g (33.4 ml, density=0.97 g/l) of 30% sodium methanolate solution and 100 ml of ethanol and the mixture is stirred at 25° C. for ca. 5 minutes; then, over the course of ca. 25 minutes, 30 g (ca. 90% strength, 180 mmol) of (1-ethoxypropylidene)malononitrile are added dropwise. The mixture is stirred for two hours, then the volatile constituents are largely removed by distillation, and the remaining residue is taken up in methylene chloride. The methylene chloride phase is separated off and the remaining 37.57 g of sodium cyano[1-(dicyanomethylidene)propyl]azanide with ca. 80% purity are used in the following stage.

후처리

  1. stirringThe mixture is stirred for two hours
  2. customthe volatile constituents are largely removed by distillation
  3. customThe methylene chloride phase is separated off

출처 및 근거

ORD 기록
ord-39e2114d5f9743aa963bd1eb88803c6f
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08329717B2

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