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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731586Generated: November 1, 2026

Acetic Acid → HCID 20227997, compound

https://huagongshe.com/reaction/1731586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium IodideHCID 5238—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 20227994HCID 20227994—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 20227997HCID 20227997—

Reaction Steps

Potassium acetate (3.0 g) then glacial acetic acid (5 ml) and then sodium iodide (1.0 g) were added to a solution of 2-chloro-1-(3,5-difluoro-4-methoxyphenyl) propan-1-one (6.5 g) in acetone (50 ml). The mixture was stirred and heated under reflux for 4 hours, cooled and treated with water (150 ml) the acetone was evaporated and the aqueous residue was extracted into dichloromethane. The organic phase was washed with sodium bicarbonate solution, dried (magnesium sulphate), and concentrated under reduced pressure, the residual oil was dissolved in ethanol (150 ml) cooled in ice and treated with excess sodium borohydride (1.5 g). The solution was stirred for 2 hours at ambient temperature, the ethanol and the residue partitioned between dilute hydrochloric acid and ethyl acetate. The ethyl acetate layer was dried (magnesium sulphate) and evaporated to give 1-(3,5-difluoro-4-methoxy-phenyl)propane 1,2-diol as an oil which was used in the next stage without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04622342
Source datasetuspto-grants-1986_11
ORD IDord-0a20ef7d9a9c407b8e6783e97ca1cf61
Source noteuspto-grants-1986_11