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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477082Generated: October 30, 2026

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

https://huagongshe.com/reaction/477082

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 numberUS04886814
Source datasetuspto-grants-1989_12
ORD IDord-f43fd102d20942c8add7410f6e89877e
Source noteuspto-grants-1989_12