Ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate → (2-Chloro-4-(trifluoromethyl)thiazol-5-yl)methanol

HRID 355026ノート

反応式

HRID 355026 の反応式
[Cl:1][C:2]1[S:3][C:4]([C:11](OCC)=[O:12])=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1.C([BH3-])#N.[Na+].[BH4-].[Na+]>C(O)C>[Cl:1][C:2]1[S:3][C:4]([CH2:11][OH:12])=[C:5]([C:7]([F:8])([F:9])[F:10])[N:6]=1

参加物

5

実験手順

To a mixture of 2.6 g (0.01 mol) of ethyl 2-chloro-4-(trifluoromethyl)-5-thiazolecarboxylate and 10 ml of ethanol was added 0.62 g of sodium cyanoborohydride. The reaction mixture was stirred for 5 minutes and 0.40 g of sodium borohydride was added. The temperature of the reaction mixture raised spontaneously to boiling point. The reaction mixture was stirred for 30 minutes and quenched with water. The aqueous mixture was extracted with ether. The ether solution was dried over CaSO4 and concentrated under reduced pressure. The residue was crystallized from petroleum ether to give 1.6 g (74%) of 2-chloro-4-(trifluoromethyl)-5-thiazolemethanol, mp 39°-45° C.

後処理

  1. temperatureThe temperature of the reaction mixture raised spontaneously
  2. stirringThe reaction mixture was stirred for 30 minutes
  3. customquenched with water
  4. extractionThe aqueous mixture was extracted with ether
  5. dry with materialThe ether solution was dried over CaSO4
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was crystallized from petroleum ether

出典と根拠

ORDレコード
ord-8334457da34d47aaaf42e126740c07d6
出典データセット
uspto-grants-1983_03
特許番号
US04377693

反応ノート

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