Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223497Generated: October 29, 2026

Methyl iodide → HCID 13067128, compound

https://huagongshe.com/reaction/223497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 136165693HCID 136165693—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 13067128HCID 13067128—

Reaction Steps

In one portion 1.0 g (2.8 mmol) of 8-chloro-6-(2-chlorophenyl)-4-methoxy-2H,4H-pyrrolo[3,4-d][2]benzazepine was added to a solution of 0.35 g (3.0 mmol) of potassium t-butoxide in 20 ml of dimethylformamide which was cooled to 0°. After stirring for 15 min, 0.3 ml (4.8 mmol) of methyl iodide was added. The mixture was stirred for 5 min, diluted with water and extracted with ether. The ether solution was washed with water, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give a pale yellow oil. Purification by column chromatography (silica gel, 25 g; 5% ether in methylene chloride, eluent) gave an off-white solid, mp 128°-130°. Recrystallization from a mixture of ether and petroleum ether gave off-white prisms, mp 128°-130°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04354973
Source datasetuspto-grants-1982_10
ORD IDord-8ec66601af024b4580a2a214afdd845f
Source noteuspto-grants-1982_10