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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Oxalyl chloride → (10-Undecenyl)phosphono chloridic acid, ethyl ester

HRID 2354492
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HRID 2354492 반응식
[CH2:1]([O:3][P:4]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH:18]=[CH2:19])(=O)[O:5]CC)[CH3:2].C(Cl)(=O)C([Cl:23])=O>C(Cl)Cl>[CH2:9]([P:4]([Cl:23])(=[O:5])[O:3][CH2:1][CH3:2])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH:18]=[CH2:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 65578Oxalyl chlorideHCID 23420214Diethyl undec-10-en-1-ylphosphonate

생성물 1

HCID 21054114(10-Undecenyl)phosphono chloridic acid, ethyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 10-undecenylphosphonic acid diethyl ester (53.51 g, 180 mmol) in CH2Cl2 (350 mL) was cooled to about −8° C. Oxalyl chloride (32 mL, 370 mmol, 2 eq.) was added slowly to the mixture, the mixture was warmed to room temperature and stirred overnight. Solvent was removed to dryness and the excess oxalyl chloride was azeotropically removed with hexane three times (100 mL). The mixture was dried in a vacuum oven at 40° C. overnight and the product was used without further purification.

후처리

  1. customSolvent was removed to dryness
  2. customthe excess oxalyl chloride was azeotropically removed with hexane three times (100 mL)
  3. customThe mixture was dried in a vacuum oven at 40° C. overnight
  4. customthe product was used without further purification

출처 및 근거

ORD 기록
ord-d5bb776de8c64176abc34fdf8b7b9c10
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07754200B2

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