HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Benzenemethanol,2-benzo[b]thien-5-yl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Benzaldehyde,2-benzo[b]thien-5-yl- | HCID 60139760 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzenemethanol,2-benzo[b]thien-5-yl- | HCID 60139743 | 93.7% |
Reaction Steps
To a suspension of 2-Benzo[b]thiophene-5-yl-benzaldehyde (compound PRE14) (3.31 g, 13.9 mmole) in methanol (30 mL) was added at 0-5° C. portionwise NaBH4 (0.528 g, 13.9 mmole). At the end of the addition, the cooling bath was removed and the reaction mixture was stirred at room temperature for 2 h. After concentration, the residue was diluted with water and diethyl ether, the organic layer dried over Na2SO4 and concentrated to give 3.13 g of compound O7 as an orange brown oil (Yield=94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981907B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-e122286ac6eb4b5e8633c656314d250f |
| Source note | uspto-grants-2011_07 |