HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485346Generated: October 29, 2026
Dimethyl Sulfoxide → 3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indole
https://huagongshe.com/reaction/485346
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | (5-Carboxypentyl)triphenylphosphanium bromide | HCID 2779280 | — |
| Reactant | HCID 13490349 | HCID 13490349 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indole | HCID 54158455 | — |
Reaction Steps
A solution of dimsyllithium (from 80 ml of dimethylsulfoxide and 13 ml of 2.1M n-butyllithium) is stirred under nitrogen at room temperature, and 6.2 g of 5-carboxypentyltriphenylphosphonium bromide is added in portions. The reaction mixture is stirred for 30 minutes and 3.0 g of N-(3-pyridyl)indole-3-carboxaldehyde is added. After 18 hours at room temperature, the reaction mixture is diluted with 240 ml of water and extracted with 100 ml of ethyl acetate. The aqueous phase is neutralized with 1.1 ml of concentrated hydrochloric acid and extracted with ethyl acetate. The extracts are dried over sodium sulfate and evaporated to an oil which is triturated with ether to give a semi-solid which is recrystallized from methanol to yield 3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indole, m.p. 124°-125°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536505 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-2dc8df6ce6464c01b10bdb1e35513d3e |
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| Source note | uspto-grants-1985_08 |
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