HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl benzo[b]thiophene-7-carboxylate → 2-(4-Methoxy-2-methyl-phenyl)-benzo[b]thiophene-7-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl benzo[b]thiophene-7-carboxylate | HCID 13759324 | — |
| Reactant | 2-(4-Methoxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl ester | HCID 57443339 | — |
| Product | 2-(4-Methoxy-2-methyl-phenyl)-benzo[b]thiophene-7-carboxylic acid methyl ester | HCID 67271921 | 12% |
Reaction Steps
The title compound (130 mg, 12%) is prepared essentially as described in the synthesis of 2-(4-methoxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl ester, utilizing benzo[b]thiophene-7-carboxylic acid methyl ester. 1H NMR (CDCl3): δ 8.08 (dd, 1H, J=7.55 Hz, 1.1 Hz), 7.97 (dd, 1H, J=7.8 Hz, 1.1 Hz), 7.48-7.42 (m, 2H), 6.87-6.79 (m, 2H), 4.03 (s, 3H), 3.85 (s, 3H), 2.48 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863302B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-87bfe7c0266147e59dd35ae8212b328b |
| Source note | uspto-grants-2011_01 |