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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246920Generated: October 31, 2026

Benzyl chloroformate → Benzyl 3-(hydroxymethyl)azepane-1-carboxylate

https://huagongshe.com/reaction/1246920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactant(Azepan-3-yl)methanolHCID 21901984—
SolventOxolane--water (1/1)HCID 21881883—
ProductBenzyl 3-(hydroxymethyl)azepane-1-carboxylateHCID 2059808694%

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium carbonate was added to a mixture of azepan-3-yl-methanol (145) (0.032 g, 0.2485 mmol) in THF/H2O (2:1, 0.31 mL). The suspension was cooled to 0° C., and (benzyloxy)carbonyl chloride (0.071 mL, 0.497 mmol) was added dropwise. The reaction was allowed to warm to room temperature overnight, and was then concentrated in vacuo. CH2Cl2 and H2O were added. The organics were extracted, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by automated silica gel chromatography with 75:25 Hexanes:EtOAc to obtain 3-Hydroxymethyl-azepan-1-carboxylic acid benzyl ester (146) in approximately 94% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129228B2
Source datasetuspto-grants-2006_10
ORD IDord-71500117350e40bf885c8952e0a52074
Source noteuspto-grants-2006_10