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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Oxalyl chloride → 5-Cyano-naphthalene-2-carboxylic acid chloride

HRID 2221291
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HRID 2221291 반응식
[C:1]([C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][C:7]([C:13]([OH:15])=O)=[CH:8]2)#[N:2].C(Cl)(=O)C([Cl:19])=O>C(Cl)Cl.CN(C=O)C>[C:1]([C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][C:7]([C:13]([Cl:19])=[O:15])=[CH:8]2)#[N:2]
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참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 69216040HCID 69216040, 화합물

생성물 1

HCID 877370955-Cyano-naphthalene-2-carboxylic acid chloride

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

To a suspension of 5-cyano-naphthalene-2-carboxylic acid, 2, (0.084 g, 0.426 mmol) in CH2Cl2 (2 mL) at room temperature containing 1 drop of DMF is added oxalyl chloride (0.074 mL). Once the solution is homogeneous, the solution is concentrated in vacuo and the crude product is used without further purification.

후처리

  1. concentrationthe solution is concentrated in vacuo
  2. customthe crude product is used without further purification

출처 및 근거

ORD 기록
ord-abfba1fb62524b74bfcd758604b4e35b
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07368462B1

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