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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451388Generated: November 1, 2026

Acetic Acid → 2-(2-Trifluoromethyl-thiazol-4-yl)morpholine

https://huagongshe.com/reaction/1451388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(2-Trifluoromethyl-thiazol-4-yl)morpholin-5-oneHCID 14076242—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Trifluoromethyl-thiazol-4-yl)morpholineHCID 19974265—

Reaction Steps

A solution of 0.9 g (0.036 mol) of 2-(2-trifluoromethyl-thiazol-4-yl)morpholin-5-one in 40 ml of tetrahydrofuran at 3° C. is mixed with 1.35 g (0.036 mol) of sodium borohydride. Then, at 5°-8° C., very slowly and with vigorous stirring 2.43 g (0.036 mol) of glacial acetic acid dissolved in 20 ml of tetrahydrofuran are added dropwise. The cooling is removed after 2 hours, and the mixture is stirred at room temperature for 16 hours. After evaporation to dryness, the resulting residue is mixed with 15 ml of 20% strength hydrochloric acid, and the mixture is heated at 90° C. for 30 minutes. It is then evaporated to dryness, the resulting product is taken up in water, and the solution is made alkaline with sodium carbonate solution. The mixture is then extracted several times with methylene chloride, the organic phase is dried over sodium sulphate and concentrated, and the residue is purified on a silica gel column using ethyl acetate/methanol=8:2 as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604225
Source datasetuspto-grants-1997_02
ORD IDord-2abfd5befc15471b952009709a237068
Source noteuspto-grants-1997_02