HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735006Generated: October 29, 2026
Carbon Dioxide → (4-pyrrolidin-1-ylmethylphenyl)propynoic Acid
https://huagongshe.com/reaction/735006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(4-Ethynylbenzyl)pyrrolidine | HCID 86060794 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (4-pyrrolidin-1-ylmethylphenyl)propynoic Acid | HCID 68819317 | — |
Reaction Steps
5.98 mL (14.85 mmol) of a 1.6M butyllithium solution in n-hexane is added dropwise to a solution of 2.3 g (12.41 mmol) of 1-(4-ethynylbenzyl)pyrrolidine in 50 mL of THF at −78° C. and stirred for 1 hour at this temperature. Then dry ice is added to the reaction mixture. Then the reaction mixture is allowed to come up to ambient temperature and stirred for 14 hours. The reaction mixture is combined with dilute hydrochloric acid and extracted with dichloromethane. The organic phase is separated off and dried over sodium sulfate. The sodium sulfate is separated off and the solvent is removed. Yield: 0.3 g (10.5% of theory); C14H15NO2 (M=229.28); calc.: molecular ion peak (M+H)+: 230; found: molecular ion peak (M+H)+: 230; Rf value: 0.15 (silica gel, dichloromethane/methanol/ammonia (9:1:0.1)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592373B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-a364a150ddeb475594ab3264fb33fcd9 |
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| Source note | uspto-grants-2009_09 |
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