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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632856Generated: November 3, 2026

1-Chloro-2-fluorobenzene → 6-Chloro-1-(2-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] maleate

https://huagongshe.com/reaction/1632856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-fluorobenzeneHCID 9583—
ReactantSodium hydrideHCID 24758—
ReactantMaleic AcidHCID 444266—
Reactant6-Chloro-1'-methylspiro[indoline-3,4'-piperidine]HCID 12801617—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product6-Chloro-1-(2-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] maleateHCID 12801626—

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of 2.4 g of 6-chloro-1'-methylspiro[indoline-3,4'-piperidine], Example 23b, 0.5 g of sodium hydride (99%) and 6 g of 2-chlorofluorobenzene in 25 ml of dimethylsulfoxide is stirred at 45° C. under nitrogen for 1 hour. Thereafter, the mixture is quenched with ice-water before being extracted thrice with ether. The combined ether extracts are successively washed with water, dried and concentrated under vacuum leaving a reddish oil. The oil is passed through an alumina column, ether eluant, and the purified oil, in ether, is converted to its maleic acid salt. The salt is recrystallized from an acetone-ether mixture to provide off-white platelets, mp 172°-173° C. of 6-chloro-1-(2-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] maleate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04477667
Source datasetuspto-grants-1984_10
ORD IDord-9f1628305c14498eaf0580b63eca5b69
Source noteuspto-grants-1984_10