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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632853Generated: November 1, 2026

1,2-Difluorobenzene → HCID 12801622, compound

https://huagongshe.com/reaction/1632853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DifluorobenzeneHCID 9706—
ReactantSodium hydrideHCID 24758—
ReactantMaleic AcidHCID 444266—
Reactant6-Chloro-1'-methylspiro[indoline-3,4'-piperidine]HCID 12801617—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
ProductHCID 12801622HCID 12801622—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 6.3 g of 6-chloro-1'-methylspiro[indoline-3,4'-piperidine], Example 23b, 1.5 g of sodium hydride, 10 g of 0-difluorobenzene and 50 ml of dimethylsulfoxide is stirred at 60° C. under nitrogen for 30 minutes. Thereafter, the mixture is permitted to cool before adding ice-water. The biphasic mixture is extracted thrice with ether. The combined ether extracts are extracted with a large excess of dilute hydrochloric acid. The acidic extract is basified with concentrated ammonium hydroxide effecting a heavy oil. The oil is purified by passing through an alumina column, ether eluant, to provide a yellowish oil. The oil, in ether, is converted to its maleic acid salt which is recrystallized from an acetone-ether mixture providing off-white crystals, mp 166°-168° C. of 6-chloro-1-(2-fluorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] maleate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04477667
Source datasetuspto-grants-1984_10
ORD IDord-fd74ea758a2a41deb74b37738531aa28
Source noteuspto-grants-1984_10