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Water → Ethyl 5-(hydroxymethyl)thiophene-2-carboxylate

HRID 2202584
ノート
印刷プレビュー

反応式

HRID 2202584 の反応式
[S:1]1[C:5]([C:6](OCC)=[O:7])=[CH:4][CH:3]=[C:2]1[C:11]([O:13][CH2:14][CH3:15])=[O:12].[BH4-].[Na+].O>C(O)C>[OH:7][CH2:6][C:5]1[S:1][C:2]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:3][CH:4]=1
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 962WaterHCID 4311764Sodium borohydrideHCID 149931952,5-Diethyl 2,5-thiophenedicarboxylate

生成物 1

HCID 24729456Ethyl 5-(hydroxymethyl)thiophene-2-carboxylate収率 52.7%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Diethyl 2,5-thiophenedicarboxylate (1.14 g, 5 mmol) synthesized in Production Example 71 was dissolved in ethanol, and sodium tetrahydroborate (113 mg, 3 mmol) was added thereto. The mixture was stirred for 3 days at a room temperature. After the completion of the reaction was confirmed by HPLC, water was added to the mixture, and the resulting mixture was concentrated under a reduced pressure. The residue was dissolved in ethyl acetate, washed with water and a saturated sodium chloride aqueous solution, and then dried over anhydrous magnesium sulfate, and the solvent was distilled off. The resulting residue was purified by flash column chromatography (Yamazen Hi-Flash column, silica gel, hexane/ethyl acetate (volume ratio)=3:2) to give the title compound (491 mg, 52.7%) as an oily substance.

後処理

  1. additionwas added to the mixture
  2. concentrationthe resulting mixture was concentrated under a reduced pressure
  3. dissolutionThe residue was dissolved in ethyl acetate
  4. washwashed with water
  5. dry with materiala saturated sodium chloride aqueous solution, and then dried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off
  7. customThe resulting residue was purified by flash column chromatography (Yamazen Hi-Flash column, silica gel, hexane/ethyl acetate (volume ratio)=3:2)

出典と根拠

ORDレコード
ord-cc59a9ca134543fcb43ab990abb755f3
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09365553B2

反応ノート

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