HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloroacetyl chloride → HCID 12923515, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hexahydro-8a-methylpyrrolo[1,2-a]pyrimidin-6(2H)-one | HCID 3161164 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12923515 | HCID 12923515 | 66.8% |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
10.5 g (0.105 mole) of triethylamine are added to a solution of 15.4 g (0.1 mole) of 6-methyl-9-oxo-1,5-diazabicyclo[4.3.0]nonane in 100 ml of toluene. The mixture is cooled to -10° C. and 14.8 g (0.1 mole) of dichloroacetyl chloride are added dropwise at from -10° to -5° C. The batch is stirred for a further 4 hours and the triethylamine hydrochloride which has precipitated is filtered off. After evaporating the toluene from the filtrate, crystals separate out, and these can be recrystallized from a 1:3 toluene/acetone mixture. 17.7 g of 5-dichloroacetyl-6-methyl-9-oxo-1,5-diazabicyclo[4.3.0]nonane, of melting point 144°-147° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04565565 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-5aaf32c3382c43699e935fb53fecfd5f |
| Source note | uspto-grants-1986_01 |