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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028171Generated: November 2, 2026

Trifluoroacetic acid → 2-Amino-6,6-dimethylfuro[3,4-d]thiazol-4(6h)-one

https://huagongshe.com/reaction/1028171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 6,6-dimethyl-4-oxo-4,6-dihydrofuro[3,4-d]thiazol-2-ylcarbamateHCID 86618914—
SolventDichloromethaneHCID 6344—
Product2-Amino-6,6-dimethylfuro[3,4-d]thiazol-4(6h)-oneHCID 87518986100.2%

Reaction Steps

To a solution of Example 5A (7.4 g, 26.0 mmol) in dichloromethane (20 mL) was added trifluoroacetic acid (20.0 ml, 260 mmol) slowly at 0° C. The reaction mixture was removed from the ice bath, allowed to reach room temperature and stirred for 3 hours. The reaction mixture was concentrated to dryness, diluted with ethyl acetate (100 mL) and neutralized with saturated NaHCO3 solution. The layers were separated and the aqueous layer was extracted with ethyl acetate (5×100 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated to give 4.8 g (99%) of product as a white solid. MS (ESI+) m/z 185 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735434B2
Source datasetuspto-grants-2014_05
ORD IDord-8bc88f3676a84eb8a20a60aff0dff2e9
Source noteuspto-grants-2014_05