Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Propenoic acid, 3-phenyl- | HCID 8784 | — |
| Reactant | Chloromethyl butanoate | HCID 2725008 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54285998 | HCID 54285998 | 72.1% |
Reaction Steps
To a stirred solution of cinnamic acid (10 g, 67 mmol) and chloromethyl butyrate (9.5 g, 1 eq) in dry dimethylformamide (25 mL) under nitrogen was dropwise added triethylamine (12 mL, 8.5 g, 1.2 eq). The reaction mixture was heated at 70° C. for 3 h; during that time a large amount of precipitate formed and TLC (ethyl acetate:hexane 1:4) showed that all the acid has reacted. The precipitate was filtered and washed with ethyl acetate. The filtrate was partitioned between water and ethyl acetate. The aqueous phase was washed with a small amount of ethyl acetate, and the combined organic phase was washed with water (3×), 5% solution of NaHCO3 (2×) and brine (2×) dried with MgSO4 and evaporated to give the crude product as an orange oil (15 g), which was distilled at 150° C./0.1-0.2 mm Hg. The pure product was obtained as a colorless oil (12 g, 72% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06124495 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-d98d36fe5d5a46cbbc3baa4612a644f7 |
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| Source note | uspto-grants-2000_09 |
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