HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 58513754, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 58513752 | HCID 58513752 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58513754 | HCID 58513754 | — |
Reaction Steps
To an ambient solution of tert-butyl 3-(2-methoxy-2-oxoethoxy)-3-(thiazol-2-yl)pyrrolidine-1-carboxylate (2.05 g, 5.99 mmol) in methanol (29.9 ml) was added NaBH4 (0.680 g, 17.96 mmol). The reaction was stirred for 1 hour and was then quenched by the addition of water (20 mL) and ethyl acetate (20 mL). The layers were separated, and the aqueous layer was extracted with additional ethyl acetate (2×20 mL). The combined organic layers were dried with anhydrous Na2SO4, filtered, and concentrated under reduced pressure to give the title compound, which was used in the subsequent step without further purification. MS ESI(+) m/z 314.9 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691810B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-ae89f94dc63b492886827a92dc0e10be |
| Source note | uspto-grants-2014_04 |