HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 13535828, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-methoxy-N-methylcarbamoyl chloride | HCID 2734926 | — |
| Reactant | HCID 13535827 | HCID 13535827 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13535828 | HCID 13535828 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
4.9 g of N-methoxy-N-methylcarbamic chloride was added drop-by-drop (over 5 minutes) to a mixture of 6.6 g of 1D, 125 ml of THF and 5.2 g of N,N-diisopropyl-N-ethylamine, at -10° C. The mixture was stirred for 1 hour at 0° C., and then mixed with ice water. The resulting mixture was extracted with ether, the extract was dried (MgSO4) and the solvent was evaporated, to give 1-(2,3-dihydro-2-methylbenzofuran-7-yl)-4-methoxy-4-methylsemicarbazide (1E), as an amber syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04577011 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-f49ff24e0d824e47998caab9fdd77aea |
| Source note | uspto-grants-1986_03 |