HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 12069561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-methoxy-2-methylindolizine | HCID 11321123 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 12069561 | HCID 12069561 | 89.8% |
Reaction Steps
1.8 ml (12.92 mmol) of triethylamine are added, at ambient temperature under an inert atmosphere, to 1.7 g (10.77 mmol) of 1-methoxy-2-methylindolizine in 15 ml of dichloroethane, followed, dropwise, by 2.2 g (11.85 mmol) of 4-nitrobenzoic acid chloride. The reaction medium is stirred for 30 minutes at ambient temperature, hydrolysed with a saturated aqueous solution of sodium hydrogen carbonate and then extracted with dichloromethane. The organic phase is washed with a saturated aqueous solution of sodium chloride, dried over sodium sulphate, and then concentrated under reduced pressure. The residue obtained is washed with diethyl ether. 3 g of an orange solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859544B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-496ba916cdec465bbfc0c7175f8647b2 |
| Source note | uspto-grants-2014_10 |