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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614188Generated: October 30, 2026

Hydrochloric Acid → HCID 21855806, compound

https://huagongshe.com/reaction/614188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl cyanoacetateHCID 7764—
Reactant3-BromotolueneHCID 11560—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178418255HCID 178418255—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 21855806HCID 2185580665.3%

Reaction Steps

To 202 ml of 2.9 M phenylmagnesium bromide in ether (0.585 mol) was aded 100 ml of ether. Then, 66.1 g (0.585 mol) of ethyl cyanoacetate was added over a few minutes with stirring at -40° to -15°. A heavy, thick precipitate formed that made stirring difficult. The mixture was allowed to warm slowly to 20°. Then, the Grignard reagent prepared from 100 g (0.585 mol) of 3-bromotoluene and 14.4 g (0.593 mol) of magnesium turnings in 300 ml of ether was added. The mixture was stirred at reflux for 4 hours, cooled, and poured slowly with stirring into 1 l. of ice-water mixture in which 62.6 g (1.17 mol) of NH4Cl was dissolved. Then, an ice-cold solution of 1.17 mol of HCl in 300 ml of water was added with stirring. The two layers were shaken together and separated. The aqueous layer was extracted with two 200-ml portions of ether. The ether layers were combined, dried (CaSO4), and concentrated under aspirator vacuum to 112.0 g of oil that contained 78.4 g (65% yield) of product (gas chromatography assay with internal standard). The oil was distilled to give 83.2 g of 89% pure product (62% yield of ester), boiling point 120°-130° (0.08 torr). Redistillation of the product through a fractionating column gave 57.2 g (48%) of 97% pure product, boiling point 118° (0.05 torr). A small sample was redistilled to give 100% pure material, boiling point 118° (0.1 torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04144047
Source datasetuspto-grants-1979_03
ORD IDord-db960153bb564626961012441d06ee7f
Source noteuspto-grants-1979_03