HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 2-Methoxycarbonyl-3-chloro4-(acetoxymethyl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Methoxycarbonyl-3-chloro4-(chloromethyl)thiophene | HCID 18376779 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Methoxycarbonyl-3-chloro4-(acetoxymethyl)thiophene | HCID 18376923 | 90% |
Reaction Steps
To 2-methoxycarbonyl-3-chloro-4-(chloromethyl)thiophene (48 g, 0.21 mol) in glacial acetic acid (500 mL) was added sodium acetate (35 g, 0.42 mol). The reaction was heated at reflux for 24 hours, then cooled and concentrated in vacuo. The residual oil was made basic by addition of saturated aqueous sodium bicarbonate, and the resulting solution extracted with ethyl acetate (4×150 mL). The combined extracts were dried over sodium sulfate and concentrated to afford 47 g (90% yield) of 2-methoxycarbonyl-3-chloro-4-(acetoxymethyl)thiophene as a light brown oil; NMR (CDCl3) 7.6 (s, 1), 5.1 (s, 2), 3.9 (s, 3), 2.1 (s, 3) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380221B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-14e39ad2b34c465a93664b1f7bfab173 |
| Source note | uspto-grants-2002_04 |