HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-Hydroxyethyl butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Hydroxyethyl butyrate | HCID 77895 | — |
Reaction Steps
As a nonlimiting example using method B in FIG. 2 to obtain the (5-oxo-1,3-oxathiolan-2-yl)methyl butanoate or its 5-acetyloxy derivative is to react 1,2-dihydroxy ethane with n-butyryl chloride in triethylamine. This reaction produces 2-hydroxyethyl butanoate, which is further reacted P2O5 in dry DCM, followed by DMSO and triethylamine to produce 2-oxyethyl butanoate. The 2-oxyethyl butanoate can be converted to the 5-acetyloxy derivative of (5-oxo-1,3-oxathiolan-2-yl)methyl butanoate by the process described above, or it can be converted into (5-oxo-1,3-oxathiolan-2-yl)methyl butanoate by reacting with mercaptoacetic acid and CSA in dry DCM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06215004B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-6d42b38dcfe14d15b8c4b59d7c239780 |
| Source note | uspto-grants-2001_04 |