HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643661Generated: October 26, 2026
Methylhydroxylamine → HCID 178482037, compound
https://huagongshe.com/reaction/643661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydroxylamine | HCID 11647 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | (1-(3-Bromophenyl)ethylidene)cyanamide | HCID 10966114 | — |
| Reactant | HCID 178481314 | HCID 178481314 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178482037 | HCID 178482037 | 83% |
Reaction Steps
To a solution of the HCl salt of methylhydroxylamine (0.19 g, 2.2 mmol, 1 eq) in ethanol (25 mL) at 25° C. was added a 21% solution of NaOEt in ethanol (0.75 mL, 2.0 mmol, 0.9 eq) followed by (1-(3-bromophenyl) ethylidene) cyanamide (0.50 g, 2.2 mmol, 1 eq). After stirring at 25° C. for 10 min, the solvent was removed in vacuo. The residue was redissolved in CH2Cl2 (25 mL), the mixture was filtered, and the solvent was removed in vacuo to give 0.5 g (83%) of 5-(3-bromophenyl)-2,5-dimethyl-1,2,4-oxadiazolidin-3-imine (DB2, R1=Me, R4=Me) as a colorless oil: 1H NMR (CDCl3) δ 7.63 (t, J=1.8 Hz, 1H), 7.52. (dd, J=2.0, 1.1 Hz, 1H), 7.38 (dd, J=2.0, 1.1 Hz, 1H), 7.29 (t, J=7.9 Hz, 1H), 3.28 (s, 3H), 1.88 (s, 3H). MS (ESI) m/e 270.0, 272.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07700603B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-b31cedebed924a7da6632adce1fcf9ca |
|---|
| Source note | uspto-grants-2010_04 |
|---|