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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429650Generated: November 1, 2026

Acetic Acid → ((2S,3R,4S)-4-amino-4-(2-fluorophenyl)-2-(trifluoromethyl)tetrahydrofuran-3-yl)methanol

https://huagongshe.com/reaction/1429650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 60169542HCID 60169542—
CatalystZincHCID 23994—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product((2S,3R,4S)-4-amino-4-(2-fluorophenyl)-2-(trifluoromethyl)tetrahydrofuran-3-yl)methanolHCID 6686928290.8%

Reaction Steps

Zinc (389.2 g, 5.95 mol) was placed in a reaction vessel, and water was added (893 mL). Acetic acid (135 mL, 2.38 mol) was added while maintaining the temperature below 10° C. After 15 min, 6a-(2-fluorophenyl)-4-(trifluoromethyl)hexahydrofuro[3,4-c]isoxazole (550.0 g, 1.98 mol) was added as a solution in THF (665 mL). The reaction mixture was stirred over 16 h at rt. Methylene chloride (1.89 L) was added, followed by 28% aq. NH4OH (552 mL) while the temperature was kept below 30° C. The mixture was stirred for 30 min, and then filtered over Celite (80 g) rinsing with methylene chloride (378 mL). The aq. layer was extracted with methylene chloride (1.89 L). The organics were combined, washed with sat. aq. NaCl (1.0 L) and concentrated under vacuum to afford an oil (502 g, 90.6%). The crude residue was used in the following step without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940734B2
Source datasetuspto-grants-2015_01
ORD IDord-5ba04cda7cbe4e4ab50f0e013fcd0820
Source noteuspto-grants-2015_01