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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733621Generated: October 30, 2026

2-Bromopropane → Methyl alpha-methylthio-alpha-(m-phenoxyphenyl)isovalerate

https://huagongshe.com/reaction/1733621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl alpha-methylthio(m-phenoxyphenyl)acetateHCID 20556696—
SolventDimethylformamideHCID 6228—
ProductMethyl alpha-methylthio-alpha-(m-phenoxyphenyl)isovalerateHCID 2055669562%

Reaction Steps

Methyl α-methylthio-(m-phenoxyphenyl)acetate (1.77 g) was dissolved in 10 ml of dimethylformamide, and with ice cooling, 260 mg (65% content) of sodium hydride was added. The mixture was stirred for 30 minutes. Then, 0.70 ml of isopropyl bromide was added, and with ice cooling for 3 minutes, the mixture was stirred at room temperature for 2.5 hours. After adding an aqueous solution of ammonium chloride (1 g/40 ml), the mixture was extracted three times with 50 ml of diethyl ether. The organic layer was washed twice with 20 ml of water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was chromatographed on a silica gel column using benzene as an eluent to afford 1.25 g of methyl α-methylthio-α-(m-phenoxyphenyl)isovalerate in a yield of 62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242519
Source datasetuspto-grants-1980_12
ORD IDord-8ff20f96d2344635bc534f213c7910cb
Source noteuspto-grants-1980_12