HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 11443332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 11329383 | HCID 11329383 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11443332 | HCID 11443332 | 88% |
Reaction Steps
A solution of [(2-{1-[4-(3,3-dimethyl-2-oxo-butoxy)-3-methyl-phenyl]-1-ethylpropyl}-benzofuran-5-carbonyl)-amino]-acetic acid (74 mg, 0.150 mmol) in THF (5.0 mL) at RT is treated with NaBH4 (11 mg, 0.300 mmol). The resulting mixture is stirred for 4 hour. The reaction is quenched with HCl (1.0 N, 1.0 mL) and extracted with EtOAc (2×20 mL). The organic layer is dried over Na2SO4, concentrated to afford the title compound (65 mg, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579488B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-7fe6a0899ca8415aaea5fd9e098e096c |
| Source note | uspto-grants-2009_08 |