HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429787Generated: October 25, 2026
Chloroacetyl chloride → 1-(Chloroacetyl)pyrrolidine
https://huagongshe.com/reaction/429787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4,5-Dimethylthiazole | HCID 62510 | — |
| Reactant | 1-(Chloroacetyl)pyrrolidine | HCID 88440 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Chloroacetyl)pyrrolidine | HCID 88440 | — |
| Product | 3-(2-(1-Pyrrolidinyl)-2-oxoethyl)-4,5-dimethyl-thiazolium chloride | HCID 9943136 | — |
Reaction Steps
3-(2-(1-pyrrolidinyl)-2-oxoethyl)-4,5-dimethyl-thiazolium chloride was prepared from the reaction of N-(chloroacetyl)pyrrolidine with 4,5-dimethylthiazole. N-(chloroacetyl)pyrrolidine was prepared as follows. Pyrrolidine (63.9 g, 0.9 mol) was taken in methylene chloride (640 mL) and cooled to 0° C. in a salt-ice bath. To the stirred mixture was added chloroacetyl chloride (101.8 g in 450 mL of CH2, Cl2, 0.9 mol) dropwise keeping the inside temperature below 15° C. After adding the chloroacetyl chloride, the mixture was stirred for an hour at 5° C. Sodium hydroxide solution (7 M, 190 mL) was added with vigorous stirring such that the inside temperature did not exceed 20° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06319934B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-ffc88bb2f5944b068e9fb000009b0ac5 |
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| Source note | uspto-grants-2001_11 |
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