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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | tert-butyl N-(4-oxocyclohexyl)carbamate | HCID 1512535 | — |
| Catalyst | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl (3-bromo-4-oxocyclohexyl)carbamate | HCID 66611191 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08912179B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-9239068aeb5a4bcab2eb70dec966b5d7 |
|---|
| Source note | uspto-grants-2014_12 |
|---|