HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoform → HCID 11773244, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Benzyl 3-pyrroline-1-carboxylate | HCID 643471 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11773244 | HCID 11773244 | — |
Reaction Steps
A solution of bromoform (0.94 mL, 10.8 mmol) in 5 mL of dichloromethane was added over 1.5 hours to a stirred solution of benzyl 3-pyrroline-1-carboxylate (1.77 mL, 9.8 mmol) and benzyltriethylammonium chloride (0.055 g, 0.025 mmol) in 1:1 dichloromethane-50% aqueous NaOH (60 mL). The black solution was stirred for 18 hours at room temperature and then diluted with dichloromethane and H2O. The layers were separated and the organic phase washed with satd NH4Cl, brine, and dried (MgSO4), filtered and concentrated. The crude product was purified by column chromatography (0-20% ethyl acetate-hexane) to afford 6,6-dibromo-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875784B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-4d6b250d35904ca3a560bcd51415ec39 |
| Source note | uspto-grants-2005_04 |