HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (+/-)-1-Propionylamino-4-hydroxymethyl-2-cyclopentene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (+-)-2-Butanol | HCID 6568 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (+/-)-2-Propionyl-2-azabicyclo[2.2.1]hept-5-en-3-one | HCID 22673281 | — |
| Solvent | Water | HCID 962 | — |
| Product | (+/-)-1-Propionylamino-4-hydroxymethyl-2-cyclopentene | HCID 22673282 | 65.3% |
Reaction Conditions
| Temperature | 10 °C |
|---|
Reaction Steps
16.6 g of (±)-2-propionyl-2-azabicyclo[2.2.1]-hept-5-en-3-one were dissolved in water (140 ml) and 2-butanol (66 ml) under nitrogen and cooled to −5° C. 3 g of sodium borohydride were added in portions over the course of 2 h. The mixture was stirred at 10° C. for 2.5 h and then adjusted to pH 2.2 with a mixture of conc. hydrochloric acid and water (1/1). The solution was evaporated to 40 g and adjusted to pH 6.2 with 2N NaOH. The mixture was extracted with 5×50 ml of dichloromethane. The combined organic phases were completely evaporated, and the residue was recrystallized in toluene (150 ml). 11.1 g of title compound were obtained. The yield was 65%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06252112B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-59e26be1319c44019ed19b3a6e7e72f2 |
| Source note | uspto-grants-2001_06 |