HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788763Generated: November 3, 2026
1,2-Dichloroethane → HCID 20190421, compound
https://huagongshe.com/reaction/1788763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 21255155 | HCID 21255155 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 20190421 | HCID 20190421 | — |
Reaction Steps
A suspension of 5-(3-pyridyl)-2,3-dihydro-1H-pyrrolizine-7-carboxylic acid (11.4 g) in a mixture of thionyl chloride (17.4 cc), dimethylformamide (0.05 cc) and 1,2-dichloroethane (150 cc) is heated at a temperature of about 80° C. for 3 hours. The reaction mixture is cooled to a temperature of about 20° C. and concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature of about 60° C. The residue obtained is suspended in cyclohexane (250 cc) and the solvent is evaporated off under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature of about 60° C. The same operation is repeated twice. 7-Chloroformyl-5-(3-pyridyl)-2,3-dihydro-1H-pyrrolizine hydrochloride (14.1 g) is thus obtained in the form of yellow crystals melting at 230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04684658 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-a0e2495416b24776b0ff2e14038ce5c9 |
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| Source note | uspto-grants-1987_08 |
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