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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Phosphorus pentachloride → (4-Cyanophenyl)methanesulfonyl chloride

HRID 1952988
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HRID 1952988 반응식
[Na].[C:2]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][S:11]([OH:14])(=O)=[O:12])=[CH:6][CH:5]=1)#[N:3].P(Cl)(Cl)(Cl)(Cl)[Cl:16]>C(#N)C>[C:2]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][S:11]([Cl:16])(=[O:14])=[O:12])=[CH:6][CH:5]=1)#[N:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24819Phosphorus pentachlorideHCID 5360545SodiumHCID 12801688HCID 12801688, 화합물

생성물 1

HCID 15480555(4-Cyanophenyl)methanesulfonyl chloride

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A suspension of 1.1 g (5.02 mMol) of the sodium salt of 4-cyanobenzenemethanesulphonic acid in 20 ml of acetonitrile was mixed with 1.2 g (5.76 mMol) of phosphorus-(V)-chloride and then refluxed for 24 hours. The insoluble matter was filtered off and the filtrate was evaporated down in vacuo. Yield; 0.8 g (74% of theory). The product was used in the next step without purification.

후처리

  1. temperaturerefluxed for 24 hours
  2. filtrationThe insoluble matter was filtered off
  3. customthe filtrate was evaporated down in vacuo
  4. customThe product was used in the next step without purification

출처 및 근거

ORD 기록
ord-a5e0cd29cb304df0be7bd304719ca75e
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06114390

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