HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632853Generated: November 1, 2026
1,2-Difluorobenzene → HCID 12801622, compound
https://huagongshe.com/reaction/1632853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Difluorobenzene | HCID 9706 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 6-Chloro-1'-methylspiro[indoline-3,4'-piperidine] | HCID 12801617 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12801622 | HCID 12801622 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04477667 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-fd74ea758a2a41deb74b37738531aa28 |
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| Source note | uspto-grants-1984_10 |
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