HuagongsheHuagongshe Chemistry Print Report · For research reference only
Crotonaldehyde → 5-(Propen-1-yl)-2-oxazoline-4-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Reactant | Ethyl isocyanoacetate | HCID 533707 | — |
| Product | 5-(Propen-1-yl)-2-oxazoline-4-carboxylic acid ethyl ester | HCID 53961155 | — |
Reaction Steps
The starting material is manufactured as follows: Reaction of crotonaldehyde with isocyanoacetic acid ethyl ester in a manner analogous to that described in Example 1 yields 5-(propen-1-yl)-2-oxazoline-4-carboxylic acid ethyl ester. By hydrolysis of the 5-(propen-1-yl)-2-oxazoline-4-carboxylic acid ethyl ester analogously to Example 1, 2-formylamino-3-hydroxy-4-hexenoic acid ethyl ester is obtained. Reaction of the 2-formylamino-3-hydroxy-4-hexenoic acidethyl ester with thionyl bromide and subsequent treatment with triethyl phosphite in a manner analogous to that described in Example 1 (12 hours) yields E-2-formylamino-5-diethylphosphono-5-methyl-3-pentenoic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05051413 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-7553fddfed5f49fab4ee741213685b75 |
| Source note | uspto-grants-1991_09 |