HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273996Erstellt: 24. Oktober 2026
3-(Bromomethyl)benzoic acid → 3-[2-Cyano-2-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]ethyl]benzoic acid
https://huagongshe.com/de/reaction/273996
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-(Bromomethyl)benzoic acid | HCID 245650 | — |
| Edukt | 3,4-Dimethoxy-alpha[(4-methylphenyl)thio]benzeneacetonitrile | HCID 10542167 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 3-[2-Cyano-2-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]ethyl]benzoic acid | HCID 10598897 | 85,1% |
Reaktionsschritte
To a cold (-78° C.) solution of 1.86 g of 3,4-dimethoxy-α-[(4-methylphenyl)thio]benzene acetonitrile in 15 mL of tetrahydrofuran is added drop-wise a solution of 2.9 mL of n-butyl lithium (2.2 M) in hexane. This solution is stirred at -78° C. for 35 minutes. A solution of 0.67 g of m-carboxybenzyl bromide in 5 mL of anhydrous tetrahydrofuran is added drop-wise, stirred at -78° C. for 40 minutes and then at room temperature for 15 minutes. The mixture is quenched with water and extracted with ethyl acetate. The ethyl acetate extract is washed with brine, dried and filtered. The filtrate is evaporated in vacuo to yield a yellow oil. This oil is purified by flash chromatography using methylene chloride/methyl alcohol (95:5) to yield 1.15 g of the desired product as a yellow foam.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05387685 |
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| Quelldatensatz | uspto-grants-1995_02 |
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| ORD ID | ord-260917c3a7ef4014bb2b71352417c94a |
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| Quellennotiz | uspto-grants-1995_02 |
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