HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (6-Methoxy-benzo[b]thiophen-2-yl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl 6-methoxybenzo[b]thiophene-2-carboxylate | HCID 11831419 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (6-Methoxy-benzo[b]thiophen-2-yl)-methanol | HCID 57608293 | 100% |
Reaction Steps
To a tetrahydrofuran (100 mL) solution of (6-methoxy-benzo[b]-thiophene-2-carboxylic acid ethyl ester (5.0 g, 21.1 mmol) described in Production Example 77-1-1 was added lithium aluminum hydride (2.0 g, 52.8 mmol). The suspension was stirred at room temperature for 30 minutes. The reaction mixture was distributed between water and ethyl acetate. The organic layer was separated followed by drying over anhydrous magnesium sulfate and filtering. The residue was concentrated under a reduced pressure to obtain the title compound (4.1 g, quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829585B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-6644c6f6b7314d86b60111c5209d7b17 |
| Source note | uspto-grants-2010_11 |