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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402667Generated: November 1, 2026

Bromine → tert-Butyl (3-bromo-4-oxocyclohexyl)carbamate

https://huagongshe.com/reaction/1402667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactanttert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
CatalystAluminum(III) ChlorideHCID 6451240—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (3-bromo-4-oxocyclohexyl)carbamateHCID 6661119167%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A solution of (4-Oxo-cyclohexyl)-carbamic acid tert-butyl ester (10 grams, 46 mmol) and aluminum chloride (0.25 grams, 2 mmol) in tetrahydrofuran (30 mL) and diethyl ether (30 mL) was cooled to 0° C., then treated with bromine (2.4 mL, 46 mmol) over a period of 30 minutes. The reaction mass was stirred for 24 hours at 0-5° C. After completion of reaction, the obtained solids were filtered and lower filtrate was concentrated under vacuum. The obtained crude was triturated with diethyl ether and the resulted solids were filtered and dried under vacuum to obtain the title compound (9.0 grams).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912179B2
Source datasetuspto-grants-2014_12
ORD IDord-9239068aeb5a4bcab2eb70dec966b5d7
Source noteuspto-grants-2014_12