HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzo[b]thiophene-3-acetic acid → 2-(Benzo[b]thiophen-3-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzo[b]thiophene-3-acetic acid | HCID 70799 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzo[b]thiophen-3-yl)ethanol | HCID 15852206 | — |
Reaction Steps
A solution of 3-benzothienylacetic acid (5.2 mmol) in 10 mL of anhydrous THF was slowly added to a stirred solution of LAH (10.4 mmol) in 50 mL of THF at 0° C. The ice bath was removed and the solution was stirred overnight, while it was allowed to warm to room temperature. The reaction was quenched by addition of water, 10% aqueous NaOH. The mixture was filtered over Celite and the filtrate was concentrated to give 2-(benzo[b]thiophen-3-yl)ethanol, which was used for tosylation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722720B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-55052d06de4a44c0b786fff16ac1eb7f |
| Source note | uspto-grants-2014_05 |