HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27411Generated: October 26, 2026
Methanol → methyl N-(2-chloroacetyl)carbamate
https://huagongshe.com/reaction/27411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Chloroacetamide | HCID 6580 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | methyl N-(2-chloroacetyl)carbamate | HCID 518783 | — |
Reaction Steps
A suspension of 2-chloroacetamide (122.6 g, 1.31 mol) in 300 ml of 1,2-dichloroethane is cooled to 0° C. and treated with oxalyl chloride (200 g, 1.57 mol). The reaction mixture is heated at reflux for 4 hours. After cooling to 5° C., 68 ml of MeOH is added dropwise while keeping the internal temperature below 15° C. with external cooling. After addition is complete, the product is separated by filtration and washed with CH2Cl2 and Et2O. Recrystallization from CH2Cl2 yields methyl(chloroacetyl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04221796 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-93e933a150fd4dfdad3e601d64c283ad |
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| Source note | uspto-grants-1980_09 |
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