HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005086Generated: October 30, 2026
Sodium Phosphate, Dibasic → 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine
https://huagongshe.com/reaction/1005086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Phosphate, Dibasic | HCID 24203 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine | HCID 10683970 | 42.1% |
Reaction Steps
A solution of 32.5 g (163 mmol) of tert-butyl 4-oxo-piperidine-1-carboxylate in 200 ml of chloroform was treated with 24.0 g (168 mmol) of disodium hydrogen phosphate and cooled to 5° C. A solution of 27.9 g (175 mmol) of bromine in 75 ml of chloroform was added dropwise during 1 hour, thereafter the reaction mixture was warmed to room temperature and stirred for 18 hours. The reaction mixture was worked-up by extraction with ice-water and methylene chloride, the organic phase was dried over magnesium sulphate, filtered and the solvent was distilled off in a water-jet vacuum. The crude product (38 g) was chromatographed on silica gel with methylene chloride and ethyl acetate as the eluent. The thus-obtained product was recrystallized from ethyl acetate and n-hexane. There were obtained 19.1 g (42% of theory) of tert-butyl 3-bromo-4-oxo-piperidine-1-carboxylate as a pale yellow solid; MS: 277, 279 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06051712 |
|---|
| Source dataset | uspto-grants-2000_04 |
|---|
| ORD ID | ord-49409d8e080b4587b3cb696877edb715 |
|---|
| Source note | uspto-grants-2000_04 |
|---|