Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 10244283 | HCID 10244283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13729867 | HCID 13729867 | 23% |
Reaction Steps
A solution of the Grignard reagent prepared from E-1-phenyl-2-(2 -bromophenyl)ethylene (8.56 g) and magnesium (0.96 g) in dry tetrahydrofuran (20 ml) was added dropwise over 30 minutes to a stirred solution of dimethyl oxalate (7.76 g) in dry tetrahydrofuran (70 ml) cooled to -15° C. The resulting mixture was stirred at about -15° C. for 30 minutes, then at room temperature for 1 hour, then poured into dilute hydrochloric acid and extracted with ether. The extracts were washed with water, dried and concentrated to give the crude product as a pale yellow oil (17.22 g). Purification by column chromatography using dichloromethane and petrol (1:1) as eluant then evaporative distillation (0.07 torr, oven temperature 170° C.) gave E-methyl 2-(2'-phenylethenyl)phenylglyoxalate (2.01 g, 23% yield) as a yellow oil, pure by GC, 1H nmr (CDCl3) : delta 3.78 (3H, s), 6.88 (centre of 2 doublets, each 1 H, J 16Hz) p.p.m.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05286894 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-886d090c56084d6889fa2b8fe239d6c5 |
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| Source note | uspto-grants-1994_02 |
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