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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506331Generated: October 28, 2026

Trifluoroacetic acid → 1-((3-(3-Phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylic acid

https://huagongshe.com/reaction/1506331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 1-((3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylateHCID 67169968—
SolventDichloromethaneHCID 6344—
Product1-((3-(3-Phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylic acidHCID 53235481—

Reaction Steps

To a stirred solution of tert-butyl 1-((3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylate (7C, 2.24 g, 4.06 mmol) in dichloromethane (4 mL) was added TFA (4 mL) slowly at room temperature. The reaction mixture was stirred at room temperature for 2 hr. The mixture was concentrated to remove dichloromethane and TFA (6 mL) was added. The mixture was stirred at room temperature till the starting material was observed to disappear. Dichloroethane (6 mL) was added and the mixture was concentrated under reduced pressure. The residue was mixed with water (10 mL), basified with 1 N aqueous NaOH to pH=8 and acidified with 1N aqueous HCl to pH=5. The mixture was sonicated for 30 min. The solid was filtered and washed with water (4×10 mL). The wet solid was mixed with methanol (40 mL), sonicated for 30 min, filtered, washed with methanol (3×10 mL), and dried to give 1-((3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-c07e994c5d1f4e8fb34afdcf888b7363
Source noteuspto-grants-2015_12