HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Ethyl 2-[1-(3'-methylaminobiphenyl-4-yl)meth-(e)-ylidene]butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 2-(diethoxyphosphoryl)butanoate | HCID 229053 | — |
| Reactant | 3'-Methylaminobiphenyl-4-carbaldehyde | HCID 1394524 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-[1-(3'-methylaminobiphenyl-4-yl)meth-(e)-ylidene]butyrate | HCID 68962496 | 72% |
Reaction Steps
197 mg (4.9 mmol) of sodium hydride are added to a mixture of 1.2 mL (4.9 mmol) of triethyl 2-phosphonobutyrate and 415 mg of 3′-methylaminobiphenyl-4-carbaldehyde (2.0 mmol) in 10 mL of tetrahydrofuran. The reaction mixture is stirred at room temperature overnight, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over sodium sulfate. The solvent is evaporated off and the residue (1.1 g) is purified by chromatography on a column of silica eluted with a 90/10 heptane/ethyl acetate mixture. 438 mg (72%) of ethyl 2-[1-(3′-methylaminobiphenyl-4-yl)meth-(E)-ylidene]butyrate are obtained in the form of off-white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383652B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-919b2e7b34d54fd6b60e8686154cb1ac |
| Source note | uspto-grants-2013_02 |