HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390668Generated: October 30, 2026
Sodium Hydroxide → 2-[1-[2-Butoxy-3'-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(e)-ylidene]butyric acid
https://huagongshe.com/reaction/390668
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-[1-[2-butoxy-3'-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(e)-ylidene]butyrate | HCID 68959502 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[1-[2-Butoxy-3'-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(e)-ylidene]butyric acid | HCID 16225010 | 76% |
Reaction Steps
40 mg (1 mmol) of sodium hydroxide are added to a solution of 531 mg (1 mmol) of ethyl 2-[1-[2-butoxy-3′-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(E)-ylidene]butyrate in 1 mL of ethanol and 10 mL of tetrahydrofuran. The reaction mixture is heated at 50° C. for 48 hours. The reaction medium is evaporated to dryness, taken up in water, acidified with aqueous 2 N hydrochloric acid solution and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over magnesium sulfate. After filtration, the solvent is evaporated off and the oil obtained is purified by chromatography on a column of silica eluted with a 60/40 heptane/ethyl acetate mixture and then precipitated from heptane. 317 mg (76%) of 2-[1-[2-butoxy-3′-(3-heptyl-1-methylureido)biphenyl-4-yl]meth-(E)-ylidene]butyric acid are obtained in the form of a white powder with a melting point of 62-64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383652B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-bf618025ad80489eb5ee9b6e6eb6211d |
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| Source note | uspto-grants-2013_02 |
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