HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bisulfate → 5-Ethyl-1,3-oxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | HCID 14474964 | HCID 14474964 | — |
| Product | 5-Ethyl-1,3-oxazolidin-2-one | HCID 13704589 | — |
| Product | 3-Ethenyl-5-ethyl-1,3-oxazolidin-2-one | HCID 14474966 | — |
Reaction Steps
3-(1-Hydroxyethyl)-5-ethyl-2-oxazolidinone is prepared from 72 g (0.626 mole) of 5-ethyl-2-oxazolidinone by the procedure described in Example 1. A total of 96 g of 3-(1-hyroxyethyl)-5-ethyl-2-oxazolidinone is obtained (87 percent conversion). The 3-(1-hydroxyethyl)-5-ethyl-2-oxazolidinone is dehydrated in the hot tube filled with steel helices which is coated with a catalyst of NaHSO4. The dehydration is conducted at 260° C. under 40 mm Hg pressure. A dark red liquid (83 g) is collected which gives 64.6 g of N-vinyl-5-ethyl-2-oxazolidinone and 10.4 g of 5-ethyl-2-oxazolidinone upon fractionation. The yield is 87 percent based on 86 percent conversion of 5-ethyl-2-oxazolidinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831153 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-2837480a0a1e448c9615fcb083fe76d5 |
| Source note | uspto-grants-1989_05 |