HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-1-benzothiophene-2-carboxylic acid → (3-Chloro-1-benzothien-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-1-benzothiophene-2-carboxylic acid | HCID 307964 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Chloro-1-benzothien-2-yl)methanol | HCID 821965 | 46% |
Reaction Steps
To an ice cold solution of 10.0 g (47.0 mmol) of 3-chloro-benzo[b]thiophene-2-carboxylic acid (11) in 200 mL of THF was added 47 mL of LiAlH4 (47 mmol, 1 M/THF). After 3 h, the reaction was quenched by addition of MeOH (ca. 40 mL). The volatiles were evaporated and the residue was treated with 50 mL 1 M HCl. After stirring for 10 min., the mixture was extracted with CH2Cl2 (3×150 mL). The combined CH2Cl2 solution was dried (MgSO4), filtered and evaporated. Purification by flash chromatography on silica gel (10-20% ethyl acetate/hexane) gave 4.32 g (21.6 mmol, 46%) of the alcohol (12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754122B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-cc73a821435b4775a26ed2b8022eaa18 |
| Source note | uspto-grants-2014_06 |