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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987396Generated: October 30, 2026

Trifluoroacetic acid → HCID 65991607, compound

https://huagongshe.com/reaction/1987396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl 3-(aminomethyl)azetidine-1-carboxylateHCID 10679125—
SolventDichloromethaneHCID 6344—
ProductHCID 65991607HCID 6599160726%

Reaction Steps

Tert-butyl 3-(aminomethyl)-1-azetidinecarboxylate (J. Med. Chem., (2001) 44:94-104) (441 mg, 2.35 mmol) was dissolved in CH2Cl2 (2 mL) and TFA (1.5 mL) and the mixture was stirred for 2 hours at room temperature. The volatiles were removed under reduced pressure and the residue was dissolved in dry MeOH (5 mL). Solid NaHCO3 was added (˜500 mg) and the mixture was stirred for 17 hours. MeOH was removed, CH2Cl2 (50 mL) was added and the mixture was filtered through a plug of Celite. The filtrate was concentrated and the residue was dissolved in DMF (15 mL). DIPEA (0.817 mL, 4.70 mmol) and 2-nitrobenzenesulfonyl chloride (580 mg, 2.58 mmol) were added and the mixture was stirred for 2 hours. The mixture was concentrated and the residue was purified by column chromatography on silica gel (100% EtOAc) to provide [1-(2-nitro-benzenesulfonyl)-azetidin-3-yl]-methanol (167 mg, 26%). 1H NMR (CDCl3) δ 2.73-2.80 (m, 1H), 3.76 (dd, 2H, J=5.4, 5.7 Hz), 3.90 (dd, 2H, J=5.7, 8.1 Hz), 4.17 (dd, 2H, J=8.1, 8.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550484B2
Source datasetuspto-grants-2009_06
ORD IDord-641fe5aafdac49ac8057517fb4ae7d3c
Source noteuspto-grants-2009_06