HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58406083, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | (E)-N-{2-[(2S)-pent-4-en-2-yloxy]ethylidene}hydroxylamine | HCID 90198734 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58406083 | HCID 58406083 | — |
Reaction Steps
To a solution of C5 (8.6 g, 0.06 mol) and triethylamine (0.455 g, 4.50 mmol) in dichloromethane (150 mL) at room temperature was slowly added a 6% aqueous solution of sodium hypochlorite (90 mL) while maintaining the internal temperature between 20° C. and 25° C. After the addition, the organic phase was separated, dried and concentrated in vacuo Silica gel chromatography (petroleum ether/ethyl acetate=10:1) provided the product as a yellow oil. Yield: 5.70 g, 40.4 mmol, 67%. LCMS m/z 142.1 [M+H+], 1H NMR (400 MHz, CDCl3), δ 4.68 (d, J=13.2 Hz, 1H), 4.59 (dd, J=10, 8 Hz, 1H), 4.18 (d, J=13.2 Hz, 1H), 3.76 (dd, J=12, 8 Hz, 1H), 3.59-3.66 (m, 1H), 3.39-3.50 (m, 1H), 2.14-2.19 (m, 1H). 1.42-1.51 (m, 1H), 1.25 (d, J=6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822456B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-09ee913218c8440ea6b025f74423a56a |
| Source note | uspto-grants-2014_09 |