HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyacetate → HCID 13080193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyacetate | HCID 5460308 | — |
| Reactant | HCID 21272614 | HCID 21272614 | — |
| Reactant | HCID 86742787 | HCID 86742787 | — |
| Product | HCID 13080193 | HCID 13080193 | 90% |
Reaction Steps
The conventional reaction of equimolar amounts of 3,5-DCI and a glycolate gives a mixture of 85-90% of an N-(3,5-dichlorophenyl)-carbamyloxyacetate (I) and 10-15% of an N,N'-bis-(3,5-dichlorophenyl)-allophanate (II), the percentages being based on 3,5-DCI employed. Both the N-(3,5-dichlorophenyl)-carbamyloxyacetate and the N,N'-bis-(3,5-dichlorophenyl)-allophanate undergo cyclization in the presence of a basic catalyst to give an N-(3,5-dichlorophenyl)-oxazolidine-2,4-dione (III), this product being obtained in a yield of about 90%, based on 3,5-DCI employed, in the case of the above mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04810799 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-3ff6dd084b4a4366b9b8a663ddc39436 |
| Source note | uspto-grants-1989_03 |