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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237259Generated: October 29, 2026

Toluene → (s)-3-[5-Chloro-2-[1-(3-trifluoromethyl-phenyl)-ethoxy]-phenoxy]-azetidine

https://huagongshe.com/reaction/237259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTrifluoroacetic acidHCID 6422—
Reactant(R)-3-[5-Chloro-2-[1-(3-trifluoromethyl-phenyl)-ethoxy]-phenoxy]-azetidine-1-carboxylic acid tert-butyl esterHCID 67349743—
SolventDichloromethaneHCID 6344—
ProductAmmonia methanolHCID 217058971%
Product(s)-3-[5-Chloro-2-[1-(3-trifluoromethyl-phenyl)-ethoxy]-phenoxy]-azetidineHCID 46214155168.4%

Reaction Steps

To the title compound of Step A (5.1 g, 10.8 mmol) in CH2Cl2 (50 mL) at 0° C. was added TFA (50 mL). After 1 h, PhCH3 (50 mL) was added and the mixture concentrated. The resulting oil was neutralized with saturated NaHCO3 (aq.) and extracted with CH2Cl2 (2×). The combined organics were dried and concentrated. Silica gel chromatography (1-7% 2M NH3/MeOH in CH2Cl2) gave 3.38 g (83% yield) of the title compound as a clear oil. MS (ESI): mass calcd. for C18H17ClF3NO2, 371.1; m/z found, 372.0 [M+H]+. 1H NMR (CDCl3): 7.70 (s, 1H), 7.56-7.53 (m, 2H), 7.45 (t, J=7.7 Hz, 1H), 6.77 (dd, J=8.6, 2.3 Hz, 1H), 6.70 (d, J=8.6 Hz, 1H), 6.55 (d, J=2.4 Hz, 1H), 5.30 (q, J=6.3 Hz, 1H), 5.00-4.94 (m, 1H), 3.97-3.93 (m, 2H), 3.89-3.81 (m, 2H), 1.66 (d, J=6.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642583B2
Source datasetuspto-grants-2014_02
ORD IDord-092d6a1ef5a6452ea655749c7c5435c7
Source noteuspto-grants-2014_02