Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methane | HCID 297 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Edukt | Butanoic acid, 4-hydroxy-, methyl ester | HCID 70217 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Methyl 4-(p-toluene-sulphonyl)-butanoate | HCID 21671020 | — |
Reaktionsschritte
25 g. Methyl 4-hydroxybutanoate were mixed with 47.5 g. toluene-sulphonyl chloride and 250 ml. dry pyridine at 5° C. and kept at this temperature for 17 hours, whereafter the reaction mixture was poured into 2 liters ice water. The oil thus formed was extracted with diethyl ether and the ethereal extract was washed with 500 ml. 6 N hydrochloric acid to remove excess pyridine, followed by washing with a saturated aqueous solution of sodium bicarbonate until neutral. Concentration of the organic layer gave 32.5 g. of a yellow oil which was dissolved in diethyl ether, treated with decolorising charcoal, filtered and the filtrate concentrated to give 30.5 g. of a pale yellow oil which slowly crystallised at 5° C. Thin layer chromatography (petroleum ether/dichloromethane/acetone 6:3:1 v/v/v) showed the product to be pure. The methyl 4-(p-toluene-sulphonyl)-butanoate thus obtained had a melting point of 23° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04190671 |
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| Quelldatensatz | uspto-grants-1980_02 |
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| ORD ID | ord-43e47ce38b9b4f3dab56503e4447474c |
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| Quellennotiz | uspto-grants-1980_02 |
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