HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922260Generated: October 26, 2026
Methanol → 3-[4-(Benzyloxy)-2-methoxyphenyl]-3-cyanopropanoic acid
https://huagongshe.com/reaction/922260
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Diethyl [4-(benzyloxy)-2-methoxybenzylidene]propanedioate | HCID 86695762 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[4-(Benzyloxy)-2-methoxyphenyl]-3-cyanopropanoic acid | HCID 66685051 | 100% |
Reaction Steps
To a 25 mL RB flask fitted with magnetic stirrer was charged with methanol (20 mL) and water (5 mL). To the stirred solvent was added diethyl [4-(benzyloxy)-2-methoxybenzylidene]propanedioate (0.775 g, 2.02 mmol), followed by potassium cyanide (0.262 g, 4.04 mmol). The RM was heated at 70° C. for 2 h. The RM was concentrated, diluted with saturated NaHCO3 solution (50 mL) and washed with ethyl acetate (50 mL×2). The aqueous layer was acidified to pH 3 with 1N hydrochloric acid and extracted with ethyl acetate (50 mL×2). The organic layer was washed with water (50 mL) and saturated brine solution (50 mL). The organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The product was obtained as brown liquid. (0.62 g, yield: 100.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278915B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-9dc5433c51c24dbca3a7f2b83180c365 |
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| Source note | uspto-grants-2016_03 |
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