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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372329Generated: October 30, 2026

Methyl iodide → 5-Chloro-N,N,2-trimethyl-3-phenyl-2H-isoindole-1-carboxamide

https://huagongshe.com/reaction/372329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 54545674HCID 54545674—
SolventDimethylformamideHCID 6228—
Product5-Chloro-N,N,2-trimethyl-3-phenyl-2H-isoindole-1-carboxamideHCID 53765504—

Reaction Steps

A suspension of 9.0 g. of 5-chloro-2-methyl-3-phenylisoindole-1-carboxylic acid methylamide in 120 ml. of dimethylformamide is treated under argon at 0° C. with 5.0 g. of potassium tert. butylate and then stirred in an ice-bath for 30 minutes. At 0°-5° C. there are added 8 ml. of methyl iodide in one batch, the mixture is subsequently stirred for 2 hours at room temperature and poured onto 2 liters of ice-water. After the addition of 100 g. of sodium chloride, the separated oil is extracted with methylene chloride. The organic phase is washed with a solution of sodium chloride, dried over sodium sulfate and concentrated to dryness under reduced pressure. The oily residue is dissolved in 200 ml. of hot hexane. The solution obtained is cooled in an ice-bath, colorless crystals separating, and there is obtained 5-chloro-2-methyl-3-phenylisoindole-1-carboxylic acid dimethylamide having a melting point of 86°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04090027
Source datasetuspto-grants-1978_05
ORD IDord-5d76b4d907c645d9b888d52ebc957509
Source noteuspto-grants-1978_05