HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 70855554, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 70855553 | HCID 70855553 | — |
| Reactant | Sodium tetraborohydride | HCID 131720822 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 70855554 | HCID 70855554 | — |
Reaction Steps
A solution of 3-bromo-4-methyl-benzo[b]thiophene-2-carboxylic acid (23c) (420 mg, 1.55 mmol) in thionyl chloride (10 mL) was refluxed for 1 hour. Thionyl chloride was then evaporated under reduced pressure and the residue was diluted with dimethoxyethane (20 mL). Sodium tetraborohydride (70 mg, 1.85 mmol) was then added to the solution. After 1 hour, the mixture was hydrolyzed with water (5 mL) and diluted with ethyl acetate (20 mL). The organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered and evaporated to dryness to afford the desired alcohol (23d) as a white solid without further purification (400 mg, 1.55 mmol, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-4d3f119bc0c44eb9aa475daca1429abf |
| Source note | uspto-grants-2016_01 |