HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839524Generated: October 29, 2026
Hydrochloric Acid → HCID 53954328, compound
https://huagongshe.com/reaction/839524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Ethylsulfamic acid | HCID 244259 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 53954328 | HCID 53954328 | 58% |
Reaction Steps
A suspension of 93.8 parts of ethylsulfamic acid and 27 parts of paraformaldehyde in 650 parts of 1,2-dichloroethane is saturated with hydrogen chloride (72 parts) at from 10° to 15° C, whilst stirring. 0.2 part of pyridine and 142.8 parts of thionyl chloride are then added in the course of 15 minutes at 15° C. The reaction mixture is stirred for 1/2 hour at 25° C and 11/2 hour under reflux. 83.5 parts of phosphorus pentachloride are then added and the mixture is stirred for 4 hours under reflux (83° C) until the evolution of gas has ceased. On concentrating under reduced pressure, and distilling, 84 parts (58% of theory) of N-ethyl-N-chloromethylsulfamic acid chloride of boiling point 70°-75° C/0.1 mbar and nD25 = 1.4800 are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04096181 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-e5e39f49da1742e0ba950e242af8ea7a |
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| Source note | uspto-grants-1978_06 |
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