HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → alpha-Nitro-beta-ethoxyacrylic acid methylester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Methyl 2-nitroacetate | HCID 17206 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Product | alpha-Nitro-beta-ethoxyacrylic acid methylester | HCID 53395203 | 84.5% |
Reaction Steps
A 12-1. three-necked flask, equipped with a thermometer, mechanical stirrer and a reflux condenser was charged under an atmosphere of nitrogen with 746 g (6.26 moles) of nitroacetic acid methylester, 1392 g (9.4 moles) of triethyl orthoformate and 1.92 l of acetic anhydride. The mixture was stirred and heated at reflux for 23 hours. The volatile components were distilled off first at atmospheric pressure (pot temperature up to 100° C., then at aspirator vacuum and finally at 0.17 mmHg (pot temperature up to 70°), leaving 926 g (84%) of crude alpha-nitro-beta-ethoxyacrylic acid methylester as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256641 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-f4cc5be488af4ae89d3ca1bd70b19add |
| Source note | uspto-grants-1981_03 |