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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579631Generated: November 3, 2026

Formaldehyde → HCID 12395600, compound

https://huagongshe.com/reaction/1579631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSulfuric AcidHCID 1118—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantHCID 12395598HCID 12395598—
ReactantHCID 12395599HCID 12395599—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 12395600HCID 12395600—

Reaction Steps

A stirred mixture of 2,3-dichloro-4-(6-bromohexanoyl)anisole (10 g.), dimethylamine hydrochloride (4 g.), paraformaldehyde (2 g.) and acetic acid (0.5 ml.) is heated on a steam bath for two hours, treated with dimethylformamide (30 ml.) and heated an additional 2 1/2 hours. The reaction mixture is poured into water, extracted with ether, washed with water and dried over magnesium sulfate. Evaporation of the ether affords 9 g. of crude 2,3-dichloro-4-(6-chloro-2-methylenehexanoyl)-anisole which is cyclialkylated by treatment with concentrated sulfuric acid (50 ml.). The sulfuric acid solution is poured into water (300 ml.) affording 5.8 g. of 2-(4-chlorobutyl)-5-methoxy-6,7-dichloro-1-indanone which melts at 92°C. after recrystallization from cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931239
Source datasetuspto-grants-1976_01
ORD IDord-e7aa5d1b03404c31bfc81431e8acf904
Source noteuspto-grants-1976_01