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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296245Generated: October 31, 2026

Methyl Acrylate → HCID 13233241, compound

https://huagongshe.com/reaction/2296245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13139564HCID 13139564—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13233241HCID 1323324164.5%

Reaction Steps

7.00 g. (16.2 mmoles) of 1-ethyl-9-bromo-1,2,3,4,6,7-hexahydro-12H-indolo[2,3-a]quinolizin-5-ium perchlorate are dissolved in 160 ml. of dichloromethane, the solution is poured into a separatory funnel, and the mixture of 28 ml. of a 10% aqueous sodium hydroxide solution and lll ml. of water is added. The two-phase mixture is shaken thoroughly, the organic phase is separated, dried over anhydrous potassium carbonate, and filtered. 8.90 g. (103.5 mmoles) of methyl acrylate are added to the filtrate, which is a dichloro-methane solution of the free base. The resulting mixture is allowed to stand at room temperature for 2 days, thereafter the solvent is evaporated in vacuo, and the oily residue is crystallized from methanol. In this way 4.70 g. (64.5%) of 1-ethyl-1-(2'-methoxycarbonylethyl)-9-bromo-1,2,3,4,6,7-hexahydro-7aH-indolo[2,3-a]quinolizin-5-ium methoxide are obtained in the form of orange red crystals; m.p.: 140°-142° C. (from methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04428877
Source datasetuspto-grants-1984_01
ORD IDord-49d948f4c1f04138be961aa0431f7b3a
Source noteuspto-grants-1984_01