HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Methyl-1-benzothiophene-6-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzo(b)thiophene-6-carboxylic acid, 2-methyl-, methyl ester | HCID 140424 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-1-benzothiophene-6-carboxylic acid | HCID 68857816 | 100% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2-Methyl-benzo[b]thiophene-6-carboxylic acid methyl ester (0.83 g, 4.0 mmol) is reacted with NaOH (0.80 g, 20 mmol) in H2O (20 mL). at reflux for 2 h. The reaction is cooled to 0° C. and acidified with 1.0 M HCl to pH (3˜4). It is extracted with EtOAc (3×100 mL); dried with Na2SO4 filtered and concentrated gives the title compound (0.78 g, 4.0 mmol, quant.). 1H NMR (CDCl3): δ 2.64 (d, J=0.89 Hz, 3H), 7.06 (s, 1H), 7.71 (d, J=8.3 Hz, 1H), 8.03 (dd, J=8.3, 1.7 Hz, 1H), 8.54 (d, J=0.8 Hz, 1H) ppm. ES-MS (m/z): calcd for C10H8O2S (M−H)−: 191.2. found: 191.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07557103B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-e4ba159c47974f2aa37060c0e0bb71b2 |
| Source note | uspto-grants-2009_07 |