HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Methyl thien-2-yl-hydroxyacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl alpha-oxo-2-thiopheneacetate | HCID 11217486 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl thien-2-yl-hydroxyacetate | HCID 13682356 | 88.4% |
Reaction Steps
To a stirred solution of methyl 2-thiopheneglyoxylate (1.01 g) in ethanol (20 ml) in an ice bath was added sodium borohydride (0.113 g) in 1 ml of water, and the mixture was stirred for 10 minutes. The reaction was quenched with aqueous acetic acid and the mixture was partitioned between methylene chloride and water. The organic extract was washed with brine, dried (sodium sulfate) and evaporated to give methyl α-hydroxy-2-thienylacetate as an oil (0.903 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05583147 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-657ee4f9087f4328a004c25ec7dafb83 |
| Source note | uspto-grants-1996_12 |