Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506330Generated: October 27, 2026

Acetic Acid → Tert-butyl 1-((3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylate

https://huagongshe.com/reaction/1506330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl azetidine-3-carboxylateHCID 21828700—
Reactant3-(3-Phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazole-7-carbaldehydeHCID 86669876—
CatalystTitanium isopropoxideHCID 11026—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
ProductTert-butyl 1-((3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylateHCID 6716996879%

Reaction Steps

To a stirred solution of 3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazole-7-carbaldehyde (7B, 2.1 g, 5.12 mmol), tert-butyl azetidine-3-carboxylate, AcOH (1.668 g, 7.68 mmol), and acetic acid (0.586 mL, 10.24 mmol) in anhydrous MeOH (10 mL) and anhydrous 1,2-dichloroethane (30 mL) was added titanium(IV) isopropoxide (3.05 mL, 10.24 mmol) dropwise at room temperature under nitrogen. The solution was stirred at room temperature for 1 hr before sodium triacetoxyborohydride (4.34 g, 20.47 mmol) was added in 10 portions over 3.5 hr. The mixture was stirred at room temperature for 2 hr. Saturated sodium bicarbonate (70 mL) was added slowly to make the mixture basic. After celite was added, the mixture was stirred at room temperature for 30 min and then filtered through a pad of celite. The aqueous filtrate was separated and extracted with dichloromethane (3×20 mL). The combined organic solutions were dried (sodium sulfate) and concentrated. Flash chromatography purification (120 g silica gel column, 25→70% ethyl acetate in hexanes) afforded tert-butyl 1-((3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)methyl)azetidine-3-carboxylate (2.24 g, 4.06 mmol, 79% yield) as a yellow solid. The compound had an HPLC retention time=3.40 min (condition C); LC/MS M+1=552.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-79673e62fae44ec3b19224b73f551580
Source noteuspto-grants-2015_12