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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283242Generated: November 1, 2026

Formaldehyde → HCID 12395600, compound

https://huagongshe.com/reaction/1283242

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 2 hours, treated with DMF (30 ml.) and heated an additional 21/2 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 numberUS03974212
Source datasetuspto-grants-1976_08
ORD IDord-977469707c0d404e8fc3e519e94e260e
Source noteuspto-grants-1976_08