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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730739Generated: October 29, 2026

Hydrochloric Acid → HCID 54085422, compound

https://huagongshe.com/reaction/1730739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl ThioglycolateHCID 16907—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14533349HCID 14533349—
Reactant4-(1-Chloroethyl)-4'-methoxy-1,1'-biphenylHCID 20348738—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventCyclohexaneHCID 8078—
ProductHCID 54085422HCID 54085422—

Reaction Steps

(4'-Methoxy-4-biphenyl)-methyl-ketone [see W. S. Johnson et al, J. Amer. Chem. Soc. 68, 1648 (1946)] was reduced with sodium borohydride to 1-(4'-methoxy-4-biphenylyl)-ethanol (m.p. 120°-122° C, from cyclohexane), and the carbinol was converted into 1-(4'-methoxy-4-biphenylyl)-1-chloroethane, m.p. 122°-124° C (from cyclohexane), with hydrogen chloride. 5.2 gm of 1-(4'-methoxy-4-biphenylyl)-1-chloroethane (0.021 mol) were admixed in 21 ml of dry dimethyl sulfoxide with 2.7 gm (0.026 mol) of thioglycolic acid methyl ester and then with 3.5 gm (0.026 mol) of dry potassium carbonate. The mixture was stirred at room temperature for 45 minutes. The reaction product was precipitated with water, suction-filtered off, washed and dried. Yield: 6.8 gm (100% of theory); m.p. 59°-61° C. A sample recrystallized from cyclohexane, analized as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03993683
Source datasetuspto-grants-1976_11
ORD IDord-ce26b216ca0a45ef814b994e543386e9
Source noteuspto-grants-1976_11