HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 57059107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 57155902 | HCID 57155902 | — |
| Product | HCID 57059107 | HCID 57059107 | — |
Reaction Steps
To 1.1 g of the (2R,3S)-3-butoxy-2-methylbutyric acid produced in the above i) was added in small portions 5 ml of oxalyl chloride at room temperature. The mixture was stirred for 2 hours at room temperature and then for 30 minutes at 50° C. Excess oxalyl chloride was removed by distillation under reduced pressure. The residue was subjected to Kugel-rohr distillation under reduced pressure to obtain 0.88 g of (2R,3S)-3-butoxy-2-methylbutyric acid chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05167863 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-ecadfdfb909b47f1bc8d33409f37c42a |
| Source note | uspto-grants-1992_12 |