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Water → 2,4-Dibromothiazole-5-methanol

HRID 577246
ノート
印刷プレビュー

反応式

HRID 577246 の反応式
[Br:1][C:2]1[S:3][C:4]([CH:8]=[O:9])=[C:5]([Br:7])[N:6]=1.[BH4-].[Na+].O>CO>[Br:1][C:2]1[S:3][C:4]([CH2:8][OH:9])=[C:5]([Br: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

5

反応物 3

HCID 962WaterHCID 36928392,4-Dibromo-thiazole-5-carbaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 100618132,4-Dibromothiazole-5-methanol収率 78.6%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a 0° C. solution of 2,4-dibromo-1,3-thiazole-5-carbaldehyde (3.38 g, 12.3 mmol) in anhydrous methanol (130 mL) was added sodium borohydride (600 mg, 15.9 mmol). The reaction mixture was stirred at room temperature for 3 hours. Water (100 mL) was added, and the mixture was evaporated. The resultant residue was extracted with EtOAc (3×100 mL). The organic extracts were combined, washed with brine (2×100 mL), dried over MgSO4, filtered, evaporated, and dried in vacuo, affording (2,4-dibromo-1,3-thiazol-5-yl)methanol (2.64 g, 77%). The product was used without further purification.

後処理

  1. customthe mixture was evaporated
  2. extractionThe resultant residue was extracted with EtOAc (3×100 mL)
  3. washwashed with brine (2×100 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customdried in vacuo

出典と根拠

ORDレコード
ord-580c5175d27e4f3eb3d5f4bc120560d2
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09040538B2

反応ノート

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