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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510935Generated: October 31, 2026

Ammonia → Benzyl 3-[3-(1-aminoethyl)-5-chloro-2-methoxy-6-methylphenyl]azetidine-1-carboxylate

https://huagongshe.com/reaction/510935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
ReactantBenzyl 3-(3-acetyl-5-chloro-2-methoxy-6-methylphenyl)azetidine-1-carboxylateHCID 86666850—
CatalystTitanium tetraethoxideHCID 76524—
ProductBenzyl 3-[3-(1-aminoethyl)-5-chloro-2-methoxy-6-methylphenyl]azetidine-1-carboxylateHCID 8666685198%

Reaction Conditions

Temperature60 °C

Reaction Steps

Titanium tetraethanolate (2.70 mL, 12.9 mmol) was added to a mixture of benzyl 3-(3-acetyl-5-chloro-2-methoxy-6-methylphenyl)azetidine-1-carboxylate (2.5 g, 6.4 mmol) in 2.0 M ammonia in ethanol (16.1 mL, 32.2 mmol) at 0° C. The solution was stirred at 60° C. under N2 overnight. Sodium tetrahydroborate (0.366 g, 9.67 mmol) was added to the above mixture at 0° C. and the solution was stirred at room temperature for another 1 hour. The reaction mixture was quenched with 2 M ammonia in water and filtered. The solid was washed with acetonitrile. The solvent was removed and the residue was diluted with dichloromethane, washed with water and brine, dried over MgSO4 and concentrated to give the desired product (2.47 g, 98%). LCMS calculated for C21H26ClN2O3 (M+H)+: m/z=389.2. found: 389.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-98bfd4a1fc2d4a989e00e4ec038878ad
Source noteuspto-grants-2015_08