HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973628Generated: November 1, 2026
Chloroacetyl chloride → HCID 21490114, compound
https://huagongshe.com/reaction/1973628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,5-Dimethylpyrrolidine | HCID 96034 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21490114 | HCID 21490114 | — |
Reaction Steps
A solution of 2,5-dimethylpyrrolidine (15 grams; 0.15 mol) and triethylamine (15 grams) in benzene (150 ml) was charged into a 250 ml glass reaction flask equipped with stirrer, reflux condenser and addition funnel. Chloroacetyl chloride (18 grams; 0.15 mol) was then slowly added, with vigorous stirring, over a period of several minutes. After the addition was completed stirring was continued for about 15 minutes. After this time the reaction mixture was filtered to remove the triethylamine hydrochloride which had formed. The filtered reaction mixture was then stripped of benzene under reduced pressure to yield a dark colored oil. The oil was distilled under vacuum to yield 1-(α-chloroacetyl)-2,5-dimethylpyrrolidine as a colorless oil having a boiling point of 89° to 90° C. at 0.1 mm of mercury pressure, and a refractive index at 25° C. of 1.4863.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03998808 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-9eebbdcd08df433eb453aa31aaf5ec11 |
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| Source note | uspto-grants-1976_12 |
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