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5-Thiazoleacetic acid, 2,4-dimethyl- → 2-(2,4-Dimethylthiazol-5-yl)ethanol

HRID 718356
ノート
印刷プレビュー

反応式

HRID 718356 の反応式
[CH3:1][C:2]1[S:3][C:4]([CH2:8][C:9](O)=[O:10])=[C:5]([CH3:7])[N:6]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH3:1][C:2]1[S:3][C:4]([CH2:8][CH2:9][OH:10])=[C:5]([CH3:7])[N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 2147995-Thiazoleacetic acid, 2,4-dimethyl-HCID 21226445Aluminium lithium hydride

生成物 1

HCID 588203362-(2,4-Dimethylthiazol-5-yl)ethanol収率 85.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 2-(2,4-dimethylthiazol-5-yl)acetic acid (230 mg, 1.343 mmol) in dry THF (10 mL) was carefully added over 2 min to solution of 2M LAH (1.343 mL, 2.69 mmol) in dry THF (10 mL) at 0° C. The reaction mixture was allowed to warm to rt and was stirred for 6 h. The reaction was quenched with 0.2 mL of water (stir for 10 min), 0.2 mL of 15% NaOH/water (stir for 10 min), and then 0.4 mL of water. After stirring for 18 h, the mixture was filtered through celite. The filtrate was concentrated in vacuum. The residue was dried under high vacuum for 16 h to afford 2-(2,4-dimethylthiazol-5-yl)ethanol (180 mg, 1.145 mmol, 85% yield) as a clear viscous oil. 1H NMR (500 MHz, CDCl3) δ 3.83 (t, J=6.3 Hz, 2H), 2.97 (t, J=6.3 Hz, 2H), 2.64 (s, 3H), 2.35 (s, 3H).

後処理

  1. customThe reaction was quenched with 0.2 mL of water (stir for 10 min), 0.2 mL of 15% NaOH/water (stir for 10 min)
  2. stirringAfter stirring for 18 h
  3. filtrationthe mixture was filtered through celite
  4. concentrationThe filtrate was concentrated in vacuum
  5. customThe residue was dried under high vacuum for 16 h

出典と根拠

ORDレコード
ord-026878e327904ced9fd99b0f3b02ac36
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09193720B2

反応ノート

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