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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702463Generated: October 31, 2026

Hydrochloric Acid → HCID 54284090, compound

https://huagongshe.com/reaction/1702463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantCalcium ChlorideHCID 5284359—
ReactantHCID 53882710HCID 53882710—
SolventMethanolHCID 887—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductHCID 54284090HCID 5428409085.9%

Reaction Conditions

Temperature-20 °C

Reaction Steps

3.05 g (0.025 mole) of calcium chloride were added to 18.1 g (0.05 mole) of 1-(2,4-dichlorophenyl)-2-(imidazol-1-yl)-3-(methylcyclohex-3-en-1-yl)-2-propen-1-one in 100 ml of methanol, and the mixture was cooled to -20° C. 1.9 g (0.05 mole) of sodium borohydride were added in portions, and, when the addition had ended, the mixture was warmed to -10° C. Thereafter, an acetone/water mixture was added dropwise and the reaction mixture was allowed to warm to room temperature. It was adjusted to a pH value of 5 with dilute hydrochloric acid and concentrated. The residue was taken up in a mixture of methylene chloride/water and the organic phase was separated off, dried over sodium sulphate, filtered and concentrated. 15.6 g (85.7% of theory) of 1-(2,4-dichlorophenyl)-2-(imidazol-1-yl)-3-(methyl-cyclohex-3-en-1-yl)-2-propen-1-ol were obtained as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04381310
Source datasetuspto-grants-1983_04
ORD IDord-7717982a5ae74b01952c8803f8061ecf
Source noteuspto-grants-1983_04