Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 14347254 | HCID 14347254 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14347316 | HCID 14347316 | 62.2% |
Reaction Steps
As in Example 115, (E)-5,5-bis(3,4-dimethoxyphenyl)-2,4-pentadienoic acid (16 g) and 4-nitrophenol (6.6 g) in dichloromethane (160 mL) was treated with 1,3-dicyclohexylcarbodiimide (9.3 g). The mixture was stirred at 0.5° C. for 1 hour, then at room temperature for 18 hours. After the usual work up, the crude product was triturated with ether to give 13.2 g of (E)-5,5-bis(3,4-dimethoxyphenyl)-2,4-pentadienoic acid 4-nitrophenyl ester. Crystallization of a portion from ether afforded the analytical sample, mp 140°-142° C. Anal. Calculated for C27H25NO8 : C, 69.60; H, 4.91; N, 3.23 Found: C, 69.19; H, 4.94; N, 3.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04975438 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-87a90cc0b09e4a50bbe7b8254c3b1919 |
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| Source note | uspto-grants-1990_12 |
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