HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660356Generated: October 31, 2026
1-Chloro-2-fluorobenzene → 6-Chloro-1-(2-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] maleate
https://huagongshe.com/reaction/1660356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-2-fluorobenzene | HCID 9583 | — |
| 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 | 6-Chloro-1-(2-chlorophenyl)-1'-methylspiro[indoline-3,4'-piperidine] maleate | HCID 12801626 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04307235 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-499e11acc4b54a8a9bb077249b753eeb |
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| Source note | uspto-grants-1981_12 |
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