Diethyl Ether → [2-(Trifluoromethyl)-1,3-thiazol-4-yl]methanol

To anhydrous ether (40 ml) was added lithium aluminium hydride (0.33 g). To this mixture was added dropwise an anhydrous ether (20 ml) solution of ethyl 2-trifluoromethyl-4-thiazole carboxylate (2 g). The mixture was stirred for 3 hours at room temperature. To the reaction mixture was added dropwise water (20 ml) under cooling with ice to decompose excess amount of the reducing agent. To the resultant reaction mixture were added ethyl acetate (50 ml) and water (25 ml), which was subjected to extraction with ethyl acetate. The organic layer was washed with water (25 ml) and a saturated aqueous solution of sodium chloride (25 ml) successively, followed by drying over magnesium sulfate. The solvent was distilled off, and the residue was subjected to a silica gel chromatography (2.5×30 cm), eluting with ethyl acetate-hexane (3:1). The desired fraction was concentrated to give 2-trifluoromethyl-4-hydroxymethylthiazole (1.1 g) as a pale yellow oily product.

1. temperatureunder cooling with ice
2. customTo the resultant reaction mixture
3. extractionwas subjected to extraction with ethyl acetate
4. washThe organic layer was washed with water (25 ml)
5. dry with materialby drying over magnesium sulfate
6. distillationThe solvent was distilled off
7. washeluting with ethyl acetate-hexane (3:1)
8. concentrationThe desired fraction was concentrated

ORDレコード

ord-ac23e9117a2341c4a75c186ede9403fe

出典データセット

uspto-grants-1995_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05405861