HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-bromoethyl ethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-bromoethyl ethanesulfonate | HCID 246381 | — |
Reaction Steps
A mixture containing 12.5 ml. of 2-bromoethanol, 12.9 ml. of ethane sulfonyl chloride and 100 ml. of ether was formed. Then, 14 ml. of triethylamine was added dropwise over a 55 minute period at 5°-10° C. and stirred for 1 hour. The mixture was allowed to come to room temperature and stirred for an additional 15 minutes. To the mixture was added 100 ml. of water, the ether layer was separated, dried over magnesium sulfate and evaporated to yield 17.6 grams of a yellow oil. nD30 1.4760.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04098599 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-184884f6af584f4fa7fe43a258fba8e5 |
| Source note | uspto-grants-1978_07 |