HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280032Generated: October 25, 2026
Acetic Acid → Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate
https://huagongshe.com/reaction/280032
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Bromocresol Green | HCID 6451 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoate | HCID 54507081 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate | HCID 20129780 | — |
Reaction Steps
A mixture of ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)-propenoate (19.8 g, 0.63 mole) in ethanol (500 mL) under nitrogen was treated with acidic acid (4 mL) and a trace of bromocresol green and heated to reflux. Heating was discontinued and sodium cyanoborohydride (4.4 g, 0.07 mole) in ethanol (100 mL) was co-added with additional acetic acid (11 mL). The mixture was stirred under nitrogen for 2 hr, acetic acid (10 mL) added and the ethanol removed under reduced pressure. The resultant yellow solid was taken up in ethyl acetate (250 mL) and successively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL), then dried over magnesium sulfate. The volatiles were removed under reduced pressure to leave an amber oil, 18.22 g (91.4%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04587342 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-5465ba6dfefa4988b66fa1857a9e3d92 |
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| Source note | uspto-grants-1986_05 |
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