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

HRID 2368014
ノート
印刷プレビュー

反応式

HRID 2368014 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 866647473-Ethoxy-4-fluoro-2-hydroxybenzaldehyde収率 65%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-eaca5ed3c232493f9073b3806df0f946
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08703742B2

反応ノート

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