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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Isopropanol → [Hydroxy(ethyl)phosphinyl]acetic acid

HRID 1028263
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HRID 1028263 반응식
[CH2:1]([P:3]([CH2:6][CH2:7][OH:8])(=[O:5])[OH:4])[CH3:2].CC(C)=[O:11].OS(O)(=O)=O.O=[Cr](=O)=O.C(O)(C)C>CC(C)=O>[CH2:1]([P:3]([OH:4])([CH2:6][C:7]([OH:11])=[O:8])=[O:5])[CH3:2]
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참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 46832563HCID 46832563, 화합물HCID 131709961Jones' reagent

생성물 1

HCID 15357685[Hydroxy(ethyl)phosphinyl]acetic acid수율 81%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

13.8 g (0.1 mol) of ethyl-(2-hydroxyethyl)phosphinic acid (produced as in Example 8) in 500 ml of acetone were admixed with 0.11 mol of Jones reagent (12.7 g of chromium trioxide in 36.7 ml of water and 11.0 ml of concentrated sulfuric acid) at 0° C. by dropwise addition. The reaction mixture was additionally stirred for 3½ hours with ice cooling and for 1 hour at room temperature. After 12 ml of isopropanol have been added, the mixture is poured onto ice-water. Volatile constituents are subsequently distilled off in vacuo. The residue was taken up in tetrahydrofuran and extracted. Insoluble salts were filtered off. The solvent of the filtrate was removed in vacuo and the residue was recrystallized from acetone to obtain 12.3 g (81% of theory) of 2-(ethylhydroxyphosphinyl)acetic acid as colorless solid.

후처리

  1. additionthe mixture is poured onto ice-water
  2. distillationVolatile constituents are subsequently distilled off in vacuo
  3. extractionextracted
  4. filtrationInsoluble salts were filtered off
  5. customThe solvent of the filtrate was removed in vacuo
  6. customthe residue was recrystallized from acetone

출처 및 근거

ORD 기록
ord-cbdc633ecbea4f15bd399a8c718cdee8
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735476B2

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