HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(diphenylmethyleneamino)acetate → (3R)-ethyl 2-(diphenylmethyleneamino)-3-ethyl-5-methylnon-8-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(diphenylmethyleneamino)acetate | HCID 319508 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (S)-5-methylnon-8-en-3-yl 4-methylbenzenesulfonate | HCID 86683255 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (3R)-ethyl 2-(diphenylmethyleneamino)-3-ethyl-5-methylnon-8-enoate | HCID 86683257 | 35.7% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
To a solution of (S)-5-methylnon-8-en-3-yl 4-methylbenzenesulfonate (15 g, 48.3 mmole) and N-(diphenylmethylene)glycinate ethyl ester (15.5 g, 58.0 mmole) in toluene (150 mL) was added LiHMDS (72.5 mL, 72.5 mmole, 1 M solution in THF) at 0° C. The reaction mass was allowed to come to room temperature heated at 110° C. for 2 h. The reaction mass was cooled to room temperature, quenched with water and extracted with ethyl acetate (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under reduced pressure to get crude compound (7.0 g, 35.7%). The crude compound was taken to the next step without further purification. MS: MS m/z 406.4 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957203B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-bdbee07400e14aaa96992b1f14262897 |
| Source note | uspto-grants-2015_02 |