HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Methyl 3-thienylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Thiophenacetic acid | HCID 23404 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-thienylacetate | HCID 94041 | — |
Reaction Steps
Acteyl chloride (7.50 ml, 106 mmol) was added dropwise to a solution of 3-thiopheneacetic acid (5.00 g, 35.3 mmol) in dry MeOH (150 ml) at 0° C. The mixture was left to slowly reach room temperature and stirred overnight. Solvents were evaporated and residue filtered through a short plug of silica gel (DCM) to give a quantitative yield of the title compound as an oil. 1H NMR (400 MHz, CDCl3): □ 3.64 (s, 2H), 3.70 (s, 3H), 7.03-7.05 (m, 1H), 7.14-7.15 (m, 1H), 7.27-7.29 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359311B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-86e5ab233536434391b1908e724c4ba2 |
| Source note | uspto-grants-2016_06 |