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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613353Generated: November 3, 2026

Ammonium Chloride → 2-Methyl-1-phenoxy-2-propanol

https://huagongshe.com/reaction/1613353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Phenoxy-2-propanoneHCID 69313—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product2-Methyl-1-phenoxy-2-propanolHCID 1037479091.4%

Reaction Steps

To a stirred solution of 24.2 g (0.16 mole) of phenoxy-2-propanone (Eastman) in 150 mL of dry ethyl ether was added 56 ml (0.17 mole) of methylmagnesium bromide (3.0M solution in ethyl ether, Aldrich) and the reaction mixture was stirred at ambient temperature under a nitrogen atmosphere for 4 hr. The reaction mixture was treated with 100 ml of saturated ammonium chloride solution and vigorously stirred for 1 hr. The layers were separated and the organic layer was washed twice with 200 ml portions of water, dried (magnesium sulfate) and the solvent evaporated under reduced pressure to yield 24.3 g (91%) of a vicous oil. A 2.3 g sample of the oil was purified by high pressure liquid chromatography (Waters Associates Prep LC/System 500 A, PrepPak® 500 silica, ethyl acetate-hexanes, 1:20, flow rate 150 ml/min). The desired fractions were combined and the solvents evaporated under reduced pressure to yield 2.1 g (91% recovery) of the title compound as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192785
Source datasetuspto-grants-1993_03
ORD IDord-0367ac7e17514cdcb590dd19caafb9d6
Source noteuspto-grants-1993_03