HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951213Generated: October 29, 2026
Dimethyl Sulfoxide → Benzyl [2-(2-oxobutylcarbamoyl)ethyl]carbamate
https://huagongshe.com/reaction/1951213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Benzyl [2-(2-hydroxybutylcarbamoyl)ethyl]carbamate | HCID 57637120 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl [2-(2-oxobutylcarbamoyl)ethyl]carbamate | HCID 57637089 | — |
Reaction Steps
To a stirred solution of oxalyl chloride (2 M in DCM) (13.35 ml, 26.5 mmol) in dry DCM at −78° C. is added dropwise DMSO (2.5 ml, 35.4 mmol). After stirring for 15 minutes, the reaction mixture is treated with a solution of [2-(2-hydroxy-butylcarbamoyl)-ethyl]-carbamic acid benzyl ester (step 1) (6.5 g, 22.1 mol) in dry DCM (40 ml). Triethylamine (13 ml) is added after 1 hour and after stirring at −78° C. for 90 minutes, the reaction mixture is allowed to warm to room temperature. The reaction is diluted with DCM (100 ml) and washed with HCl (1M, 200 ml), saturated sodium bicarbonate solution (200 ml), water (200 ml) and brine (200 ml). The organic portion is dried over MgSO4, filtered and concentrated in vacuo to yield the titled compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08404684B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-261b6998026f41909e4931c5cc509ae2 |
|---|
| Source note | uspto-grants-2013_03 |
|---|