HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofurfuryl alcohol → HCID 23286429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromopropanoyl chloride | HCID 97980 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23286429 | HCID 23286429 | 94% |
Reaction Steps
To a 250 milliliter three-necked flask were added 0.15 mole of 2-(hydroxymethyl)tetrahydrofuran, 0.15 mole of triethylamine, and 100 milliliters of diethylether. The flask was immersed in ice, and 0.15 mole of 2-bromopropanoyl chloride introduced dropwise. The ice bath was removed, and the reaction stirred at ambient temperature for two hours. The mixture was extracted with an equal volume of water, and the organic phase dried over sodium sulfate. Decantation and solvent removal resulted in 2-tetrahydrofuranylmethyl 2-bromopropanoate in 94% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120348 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-1336cb574257428eaae86f72af593f03 |
| Source note | uspto-grants-1992_06 |