HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 5-(chloromethyl)thiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methyl 5-(hydroxymethyl)thiophene-3-carboxylate | HCID 12926498 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-(chloromethyl)thiophene-3-carboxylate | HCID 12926494 | 46.2% |
Reaction Steps
A solution of 5-hydroxymethyl-thiophene-3-carboxylic acid methyl ester (8.8 g, 51.1 mmol) and triethylamine (7.8 mL, 56.2 mmol) in dichloromethane (135 mL) is cooled to 0° C. and treated with a solution of thionyl chloride (4.1 mL, 56.2 mmol) in dichloromethane (40 mL) in a dropwise maner. After stirring for 1 h, water is added and the mixture is extracted with dichloromethane. The combined organics are dried over Na2SO4, filtered and concentrated in vacuo. The residue is purified by flash chromatography (silica gel, 10% ethyl acetate in heptane) to give 5-chloromethyl-thiophene-3-carboxylic acid methyl ester (4.5 g, 46%) an amber oil. 1H NMR (CDCl3, 300 MHz) δ 8.04 (s, 1 H), 7.43 (s, 1 H), 4.78 (s, 2 H), 3.84 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361671B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-09b17c348c0b4865bc421f4de6824b91 |
| Source note | uspto-grants-2008_04 |