HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903004Generated: October 25, 2026
Allyl chloride → Ethyl [(prop-2-en-1-yl)oxy]carbamate
https://huagongshe.com/reaction/903004
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Hydroxyurethane | HCID 11510 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl [(prop-2-en-1-yl)oxy]carbamate | HCID 19860187 | — |
Reaction Steps
100 g of N-hydroxyurethane and 80.3 g of allyl chloride were added, at 20° C., to a solution of 53.8 g of potassium hydroxide in 750 ml of ethanol. The mixture was stirred and refluxed (80° C.) for 4 hours, then was cooled to 25° C. and filtered. The solvent was evaporated from the filtrate and the residue, an oil, was distilled, 51°-55° C., 0.2 Torr., to give ethyl (2-propenyloxy)carbamate, 3A, as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04226612 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-0eda31aec55b414b8acdd83dfd38cd52 |
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| Source note | uspto-grants-1980_10 |
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