HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650198Generated: October 27, 2026
Phenylethanolamine → 2-Nitromethylene-5-phenyl-oxazolidine
https://huagongshe.com/reaction/1650198
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylethanolamine | HCID 1000 | — |
| Reactant | 1,1-Bis(methylthio)-2-nitroethylene | HCID 83623 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-Nitromethylene-5-phenyl-oxazolidine | HCID 67897166 | 56.5% |
Reaction Steps
In a mixture of 60 ml of ethanol and 200 ml of xylene was dissolved 40 g of DL-β-hydroxyphenethylamine, and the resulting solution was added dropwise to a solution of 57.8 g of 1,1-bis(methylthio)-2-nitroethene in 600 ml of xyelene under reflux over a period of 1.5 hours to effect reaction. During the reaction, the low-boiling fractions were gradually removed by distillation and the reaction temperature was maintained at 130° C. to 140° C. After completion of the reaction, crystals were deposited with stirring under ice-cooling. The crystals deposited were collected by filtration, dried, and then mixed with 200 ml of a 5% (by weight) aqueous sodium hydroxide solution. After a slight amount of insolubles were removed by filtration, the filtrate was adjusted to pH 6 with a 10% (by weight) aqueous acetic acid solution, and the crystals deposited were collected by filtration and dried to obtain 34 g of 2-nitromethylene-5-phenyloxazolidine having a melting point of 139°-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04923882 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-37c8867c07e9439997b9b164440b42a9 |
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| Source note | uspto-grants-1990_05 |
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