HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 14821670, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic-formic anhydride | HCID 75269 | — |
| Reactant | HCID 14821669 | HCID 14821669 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14821670 | HCID 14821670 | — |
Reaction Steps
To a mixture of (E)-3-fluoro-3-hexylsulfinyl-2-propenol (0.21 g, 1.0 mmol) and 2 ml of pyridine cooled to -30° is added through syringe acetic-formic anhydride (0.4 ml). The mixture is allowed to warm to 10° over a period of 1 hour. It is then diluted with water, extracted with hexane, washed with aqueous 2N H2S04, then water, then aqueous NaHCO3, finally brine and is dried. The product is purified by prep. TLC to give (E)-3-fluoro-3-hexylsulfinyl-2-propenyl formate (cpd. 3, Table A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04877899 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-f4aad9cd2cf441d7b0bb4cf680a8ca88 |
| Source note | uspto-grants-1989_10 |