Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487951Generated: October 27, 2026

Triethylamine → Tert-butyl 4-bromo-5-oxoazepane-1-carboxylate

https://huagongshe.com/reaction/1487951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantN-Boc-hexahydro-1H-azepin-4-oneHCID 1512679—
SolventChloroformHCID 6212—
ProductTert-butyl 4-bromo-5-oxoazepane-1-carboxylateHCID 5914377427%

Reaction Steps

To a solution tert-butyl 4-oxoazepane-1-carboxylate (compound 82.2, 11.0 g, 51.6 mmol) in chloroform (220 mL) at 0° C. was added drop-wise a solution of bromine (3.98 mL, 77.6 mmol) in chloroform (110 mL). The resulting mixture was stirred at room temperature overnight, then the solids that formed were collected by filtration and dissolved in dichloromethane (200 mL). Triethylamine (16.8 mL, 121 mmol) and (Boc)2O (8.70 g, 40.3 mmol) were added to the mixture at 0° C. and the resulting solution was stirred for 3 h at room temperature, and then concentrated under reduced pressure. The crude residue was purified by silica gel chromatography using ethyl acetate/petroleum ether (1:10) as the eluent to give 4.0 g (27%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428502B2
Source datasetuspto-grants-2016_08
ORD IDord-fffbe8dbe9284d598c9f637c8e2e35ca
Source noteuspto-grants-2016_08