HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Ethyl 2-(2-chloro-4-iodo-benzoyl)-3-ethoxy-acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Ethyl 3-(2-chloro-4-iodo-phenyl)-3-oxo-propionate | HCID 19081721 | — |
| Product | Ethyl 2-(2-chloro-4-iodo-benzoyl)-3-ethoxy-acrylate | HCID 53916769 | 90% |
Reaction Steps
md) 53.7 g of ethyl 3-(2-chloro-4-iodo-phenyl)-3-oxo-propionate are heated to boiling under reflux for 4 hrs. with 40 g of triethyl orthoformate and 46.1 g of acetic anhydride. The volatile constituents are distilled off in a water-jet vacuum and finally in a high vacuum. 55.9 g (90%) of ethyl 2-(2-chloro-4-iodo-benzoyl)-3-ethoxy-acrylate are obtained as a yellowish oil. Mass spectrum: peaks inter alia at 408 (M+, 4%), 373 (67%), 342 (14%), 335 (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763450 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-f30372f5d3ff4c65a6638ec5f0321b17 |
| Source note | uspto-grants-1998_06 |