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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(2-Trifluoromethyl-thiazol-4-yl)morpholin-5-one | HCID 14076242 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Trifluoromethyl-thiazol-4-yl)morpholine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04886814 |
|---|
| Source dataset | uspto-grants-1989_12 |
|---|
| ORD ID | ord-f43fd102d20942c8add7410f6e89877e |
|---|
| Source note | uspto-grants-1989_12 |
|---|