HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 5-(hydroxymethyl)thiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-(Hydroxymethyl)thiophene-3-carboxylic acid | HCID 59698814 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-(hydroxymethyl)thiophene-3-carboxylate | HCID 12926498 | 56% |
Reaction Steps
A mixture of 5-hydroxymethyl-thiophene-3-carboxylic acid (14.5 g, 91.7 mmol), concentrated H2SO4 (5.2 mL, 93.5 mmol) and methanol (250 mL) is heated to reflux for 3.5 h. After cooling, the mixture is poured into water and extracted with dichloromethane (3×). The combined extracts are washed successively with saturated aq NaCl, aq NaHCO3 and water followed by drying over Na2SO4, filtration and concentration in vacuo. The residue is purified by distillation to give 5-hydroxymethyl-thiophene-3-carboxylic acid methyl ester (8.8 g, 56%) as a clear oil: bp 155-157° C./6-7 mbar; 1H NMR (CDCl3, 300 MHz) δ 7.98 (s, 1 H), 7.35 (s, 1 H), 4.78 (s, 2 H), 3.80 (s, 3 H), 2.63 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361671B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-3dd799c5a07f4d37b79975286dcbaaa3 |
| Source note | uspto-grants-2008_04 |