HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268455Generated: October 25, 2026
Dimethylformamide → Ethyl 2-(4-benzyloxyphenyl)-3-(6-bromo-2,3,4,5-tetramethoxyphenyl)-2-ethoxycarbonylpropionate
https://huagongshe.com/reaction/2268455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl 2-(4-(benzyloxy)phenyl)malonate | HCID 2823246 | — |
| Reactant | 1-Bromo-6-bromomethyl-2,3,4,5-tetramethoxybenzene | HCID 18348620 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-(4-benzyloxyphenyl)-3-(6-bromo-2,3,4,5-tetramethoxyphenyl)-2-ethoxycarbonylpropionate | HCID 18348651 | 49.6% |
Reaction Steps
A DMF (120 ml) suspension of ethyl 2-(4-benzyloxyphenyl)-2-ethoxycarbonylacetate (12.0 g, 35.1 mmols), 1-bromo-6-bromomethyl-2,3,4,5-tetramethoxybenzene (16.9 g, 45.6 mmols) and potassium carbonate (14.5 g, 105 mmols) was stirred at room temperature for 6 hours, and then 1-bromo-6-bromomethyl-2,3,4,5-tetramethoxybenzene (2.60 g, 7.02 mmols) was added thereto stirring was continued at room temperature for further 6 hours. Water was added to the reaction mixture, which was then extracted with diethyl ether. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and then dried. The solvent was evaporated out in vacuo, and the resulting crude product was purified by recrystallization (from hexane-ethyl acetate) to obtain the entitled compound (11.0 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326369B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-84c101868c234a6ea17a0a5ae58899ec |
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| Source note | uspto-grants-2001_12 |
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