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Hydrochloric Acid → 3-Ethoxy-4-fluoro-2-hydroxybenzaldehyde

HRID 2368014
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HRID 2368014 반응식
[OH:1][C:2]1[C:9]([OH:10])=[C:8]([F:11])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].I[CH2:13][CH3:14].Cl>CS(C)=O>[CH2:13]([O:10][C:9]1[C:2]([OH:1])=[C:3]([CH:6]=[CH:7][C:8]=1[F:11])[CH:4]=[O:5])[CH3:14]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6340IodoethaneHCID 451191034-Fluoro-2,3-dihydroxybenzaldehyde

생성물 1

HCID 866647473-Ethoxy-4-fluoro-2-hydroxybenzaldehyde수율 65%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To a solution of 2,3-dihydroxy-4-fluorobenzaldehyde (3.0 g, 19.23 mmol) in DMSO (100 mL), NaOBu-t (3.692 g, 38.46 mmol) was added in portions at room temperature and stirred for 15 min. Then iodoethane was added dropwise at room temperature and stirred for 18 h. The reaction mixture was poured onto crushed ice (200 mL) and acidified with 2.5 M HCl to pH 3.0. The product was extracted with ethyl acetate (2×100 mL), concentrated and the product was chromatographed on a column of silica gel (Hex:EtOAc=95:5) to give the title compound as a crystalline solid (2.3 g, 65%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm: 11.36 (s, 1H), 9.83 (s, 1H), 7.39-7.19 (m, 1H), 6.77 (t, J=9.2 Hz, 1H), 4.22 (q, J=7.0 Hz, 2H), 1.40 (t, J=7.0 Hz, 3H); MS (ESI) m/z=183 (M+1, positive).

후처리

  1. stirringstirred for 18 h
  2. additionThe reaction mixture was poured
  3. extractionThe product was extracted with ethyl acetate (2×100 mL)
  4. concentrationconcentrated
  5. customthe product was chromatographed on a column of silica gel (Hex:EtOAc=95:5)

출처 및 근거

ORD 기록
ord-eaca5ed3c232493f9073b3806df0f946
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08703742B2

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