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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16602Generated: October 25, 2026

Benzyl Alcohol → tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate

https://huagongshe.com/reaction/16602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium IodideHCID 5238—
Reactant3-Chloro-2,2-dimethylpropanoyl chlorideHCID 61345—
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
ReactantBenzyl 3-chloropivalateHCID 54294282—
SolventDimethylformamideHCID 6228—
Producttert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamateHCID 866021211.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirred solution of tert-butyl (piperidin-4-ylmethyl)carbamate (38.8 g, 181 mmol) in N,N-dimethylformamide (100 mL) was added benzyl 3-chloropivalate {14.2 g, 124 mmol, prepared from 3-chloropivaloyl chloride (25.6 g, 165 mmol) and benzyl alcohol (19.6 g, 181 mmol), ethyldiisopropylamine (64.0 g, 495 mmol) and sodium iodide (27.1 g, 181 mmol) at ambient temperature. The resulting mixture was stirred at 120° C. for 14 h. The volatile components were removed by evaporation and the resulting residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 640 mg (1%) of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737163B2
Source datasetuspto-grants-2010_06
ORD IDord-51017605c27a4df0905c4c42548db89d
Source noteuspto-grants-2010_06