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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652776Generated: October 30, 2026

Acetone → HCID 86741589, compound

https://huagongshe.com/reaction/652776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 54502136HCID 54502136—
ReactantHCID 86681511HCID 86681511—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 86741589HCID 86741589—

Reaction Steps

4.9 g of 2-methoxy-4-amino-5-ethyl sulphonyl benzoic acid, 57 ml of acetone, 10 ml of water and 2.6 ml of triethylamine (density 0.726) are placed in a 250 ml flask fitted with an agitator, a thermometer, a condenser and a dropping funnel. The solution is cooled to between 0° and +5° C. and 2.1 g of ethyl chloroformate is added drop by drop. The reaction medium is agitated for 45 minutes at room temperature then cooled to 0° C. and 5.3 g of 1-cycloheptyl methyl-2-amino methyl pyrrolidine is poured in drop by drop. The medium is agitated for 4 hours then left to stand overnight. The solvents are evaporated to dryness and the residue is dissolved in 60 ml of water and 15 ml of hydrochloric acid (density 1.18). Extraction is carried out 3 times with 50 ml of methylene chloride, the organic phase is dried over magnesium sulphate and filtered, and the solvent is evaporated under vacuum. The residue is dissolved in 100 ml of water. The solution is filtered in the presence of carbon black and the filtrate is made alkaline with about 7 ml of ammonia (density 0.91). A gum is precipitated. It is extracted 3 times with 50 ml of methylene chloride. The organic phase is washed twice with 50 ml of water, dried over magnesium sulphate and filtered. The solvent is evaporated under vacuum and the residue is re-crystallised in 100 ml of isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04673686
Source datasetuspto-grants-1987_06
ORD IDord-2df1bb6728664843bb0ad2982a648a47
Source noteuspto-grants-1987_06