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4-Nitrobenzaldehyde → HCID 10661075, 화합물

HRID 350719
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HRID 350719 반응식
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].[PH2:12]([O:14][CH2:15][CH3:16])=[O:13].C(N(CC)CC)C.C([O:27][CH2:28][CH3:29])(=O)C>>[OH:9][CH:8]([P:12](=[O:13])([O:27][CH2:28][CH3:29])[O:14][CH2:15][CH3:16])[C:7]1[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 5414-NitrobenzaldehydeHCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 178476775HCID 178476775, 화합물

생성물 1

HCID 10661075HCID 10661075, 화합물

실험 절차

To a mixture of 4-nitrobenzaldehyde (8.56 g) and ethyl hypophosphite (7.81 g) was gradually added triethylamine (1.5 mL). After stirring for 1 hr., the reaction mixture was diluted with ethyl acetate and washed successively with 1N hydrochloric acid and water. The organic layer was dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography, and diethyl α-hydroxy-4-nitrobenzylphosphonate was obtained as crystals from a fraction eluted with ethyl acetate-hexane (1:1, volume ratio). Recrystallization from ethyl acetate-hexane gave yellow prism crystals (4.62 g, yield 28%). melting point: 94–95° C.

후처리

  1. washwashed successively with 1N hydrochloric acid and water
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-44ecfd4c70d145ad967c24426bde536e
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07183276B2

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