HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 23371323, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzaldehyde, 4-(phenylmethoxy)- | HCID 78109 | — |
| Reactant | HCID 20153620 | HCID 20153620 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23371323 | HCID 23371323 | 48% |
Reaction Steps
A solution of 3.0 g (10 mmol) of dimethyl (E)-2-(1-methoxy-2-methoxycarbonylethenyl)benzylphosphonate and 2.1 g (10 mmol) of 4-benzyloxybenzaldehyde in 50 ml of dimethylformamide is added dropwise at room temperature to 0.26 g (11 mmol) of NaH in 20 ml of dimethylformamide. The mixture is stirred for 3 h, and then NH4Cl solution is added. After extraction with ethyl acetate, the organic phase is washed with water, dried over Na2SO4 and concentrated. Recrystallization from diisopropyl ether/n-hexane results in 1.9 g (48%) of pale yellow crystals of methyl 2-[2-(4-benzyloxyphenyl)-(E)-ethenyl]-(E)-β-methoxycinnamate of melting point 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538940 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-fc5180aa944f4766aa76f502205fee64 |
| Source note | uspto-grants-1996_07 |