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Ethanol → Ethyl [3-(hydroxymethyl)phenoxy]acetate

HRID 979543
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HRID 979543 반응식
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][CH:13]=1)[O:6][CH2:7][C:8]([OH:10])=[O:9].C(Cl)(Cl)Cl.O.[CH2:19](O)[CH3:20]>S(=O)(=O)(O)O>[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:11]=[CH:12][CH:13]=1)[O:6][CH2:7][C:8]([O:10][CH2:19][CH3:20])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 962WaterHCID 6212ChloroformHCID 246028[3-(Hydroxymethyl)phenoxy]acetic acid

생성물 1

HCID 18367402Ethyl [3-(hydroxymethyl)phenoxy]acetate

시약·촉매·용매 1

HCID 1118Sulfuric Acid촉매

실험 절차

A solution of 3-(hydroxymethyl)phenoxyacetic acid (3.18 g.) in ethanol (30 ml.) was treated with concentrated sulphuric acid (10 drops) and allowed to stand for 3 days. Chloroform (100 ml.) and water (50 ml.) were then added. The organic phase was separated, washed sequentially with saturated aqueous sodium hydrogen carbonate solution (2×50 ml.), water (50 ml.) and saturated brine (50 ml.) and then dried (MgSO4) The dried solution was evaporated and the residue purified by flash column chromatography, eluting with petrol (40°-60° )/ ethyl acetate (60:40 v/v) to give ethyl 3-(hydroxymethyl)phenoxyacetate (2.6 g.) as a colourless oil, NMR: 1.25 (3H,t), 2.8 (1H,br s), 4.25 (2H,q), 4.6 (4H,s) and 6.6-7.4 (4H,m)ppm.

후처리

  1. customThe organic phase was separated
  2. washwashed sequentially with saturated aqueous sodium hydrogen carbonate solution (2×50 ml.), water (50 ml.) and saturated brine (50 ml.)
  3. dry with materialdried (MgSO4) The dried solution
  4. customwas evaporated
  5. customthe residue purified by flash column chromatography
  6. washeluting with petrol (40°-60° )/ ethyl acetate (60:40 v/v)

출처 및 근거

ORD 기록
ord-596e1f7cd91f43478f86513da932557b
출처 데이터셋
uspto-grants-1987_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04668698

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