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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652768Generated: October 31, 2026

Citric Acid → HCID 86741585, compound

https://huagongshe.com/reaction/652768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 20196828HCID 20196828—
ReactantHCID 86741586HCID 86741586—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 86741585HCID 86741585—

Reaction Conditions

Temperature20 °C

Reaction Steps

53.5 g of 2-methoxy-5-methyl sulfinyl benzoic acid, 740 ml of acetone, 140 ml of water and 35 ml of triethylamine (density 0.726) are placed in a 2 liter flask fitted with an agitator, a thermometer and a dropping funnel. The solution is cooled to between 0° and +5° C., after which 34.1 g of isobutyl chloroformate is dripped in. The mixture is agitated for 45 minutes at 20° C. then cooled to 0° C., and 42 g of 1-cyclopropyl-2-amino methyl pyrrolidine is poured in drop by drop. The mixture is reacted at room temperature then left to stand. The solvents are evaporated under vacuum. The oily residue is dissolved in 250 ml of water and 50 ml of hydrochloric acid (density 1.18) and extracted twice with 125 ml of methylene chloride. The aqueous phase is then made alkaline with 70 ml of soda lye. A yellow oil is salted out. It is extracted 3 times with 250 ml of methylene chloride and the organic phase is washed 3 times with 100 ml of water and dried over magnesium sulphate. The solution is filtered and the solvent evaporated. An oily residue is obtained. It is dissolved in 500 ml of ethanol and an equimolar quantity of citric acid is added. It is evaporated under vacuum and the residue is dissolved in 1,000 ml of boiling isopropanol then cooled. The supernatant solution is decanted off and the residual paste dissolved in 600 ml of water. The solution is filtered with charcoal then the filtrate is evaporated under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04673686
Source datasetuspto-grants-1987_06
ORD IDord-d6b1590e657044bfa3931ad25e06827b
Source noteuspto-grants-1987_06