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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (R)-3-[5-Chloro-2-[1-(3-trifluoromethyl-phenyl)-ethoxy]-phenoxy]-azetidine-1-carboxylic acid tert-butyl ester | HCID 67349743 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonia methanol | HCID 21705897 | 1% |
| Product | (s)-3-[5-Chloro-2-[1-(3-trifluoromethyl-phenyl)-ethoxy]-phenoxy]-azetidine | HCID 46214155 | 168.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642583B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-092d6a1ef5a6452ea655749c7c5435c7 |
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| Source note | uspto-grants-2014_02 |
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