HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl bromoacetate → Tert-butyl (methylthio)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | Methylmercaptan sodium | HCID 45051789 | — |
| Product | Tert-butyl (methylthio)acetate | HCID 10241116 | 96.5% |
Reaction Steps
Under ice cooling, 33.4 g of tert-butyl bromoacetate was gradually added to 80.0 g of 15% sodium methylmercaptan aqueous solution and the resulting mixture was reacted at room temperature overnight. After completion of the reaction, the reaction mixture was extracted 4 times with ethyl acetate and the extract was washed with saturated sodium chloride aqueous solution. After the ethyl acetate layer was dried over magnesium sulfate, ethyl acetate was distilled off to give 26.8 g of crude tert-butyl (methylthio)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05233035 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-615ec9bb67ae47e998ccd34723eb8455 |
| Source note | uspto-grants-1993_08 |