HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Oxo-1,3-thiazolidine-4-carboxylic acid → N-(3-Nitrooxypropyl)-2-oxothiazolidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Oxo-1,3-thiazolidine-4-carboxylic acid | HCID 65272 | — |
| Reactant | 3-Nitroxypropylamine nitrate | HCID 22014591 | — |
| Product | N-(3-Nitrooxypropyl)-2-oxothiazolidine-4-carboxamide | HCID 18961065 | 35.4% |
Reaction Steps
A procedure similar to that described in Example 1 was repeated, but using 1.25 g of N-(3-nitrooxypropyl)amine nitrate and 1.0 g of 2-oxothiazolidine-4-carboxylic acid, to obtain 0.60 g of the title compound as pale yellow crystals, melting at 83°-850° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05356918 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-6839537b56b64bbd9fd75bbb4d5e8a12 |
| Source note | uspto-grants-1994_10 |