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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121006Generated: October 30, 2026

Benzhydrylamine → HCID 69028747, compound

https://huagongshe.com/reaction/2121006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylamineHCID 7036—
Reactant1-Benzylpiperidin-4-olHCID 78461—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl chloroformateHCID 82129—
SolventAcetonitrileHCID 6342—
ProductHCID 69028747HCID 6902874750%

Reaction Steps

1-Benzyl-4-piperidinol (2.09 g, 10.9 mmol) and 4-nitrophenyl chloroformate (2.2 g, 10.9 mmol) were dissolved in anhydrous acetonitrile (10 mL). To this solution was added diisopropylethylamine (1.4 g, 10.9 mmol) and the resulting yellow solution was stirred at room temperature. After 3 h, aminodiphenylmethane (2 g, 10.9 mmol) was added and the reaction mixture was heated at 65° C. After 3 h, the reaction mixture was cooled to room temperature and stirred for an additional 12 h. The resulting solid was filtered, washed with cold acetonitrile to give 1-benzyl-4-piperidylbenzhydryl carbamate (1.3 g, 50%) as a colorless solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693202B1
Source datasetuspto-grants-2004_02
ORD IDord-05bedc54bb5047e3b22323a9cd2ea843
Source noteuspto-grants-2004_02