Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | 4-Methylbenzenethiol | HCID 7811 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 14738-27-3 | HCID 271492 | 99% |
Reaktionsschritte
A solution of 4-methylbenzenethiol (5 g, 40.25) in dry THF was added dropwise to a suspension of NaH (60% in mineral oil, 1.98 g, 48.30) in THF at room temperature and stirred for 30 min. under N2 atmosphere. Ethylbromoacetate (4.9 mL, 44.27) was added slowly to this solution and further stirred at room temperature for 3 h. The solvent was removed under vacuum. The residue was dissolved in dil. HCl and extracted by ethylacetate. The combined organic phase was washed successively with saturated NaHCO3 solution, water and brine then dried over Na2SO4. Evaporation of organic phase yielded 8.46 g (99%) colorless oil. 1H NMR (CDCl3): δ 1.22 (t, J=7.2 Hz, 3H), 2.32 (s, 3H), 3.57 (s, 2H), 4.14 (q, J=7.2 Hz, 2H), 7.11 (d, J=8.0 Hz, 2H), 7.33 (d, J=8.0 Hz, 2H). EIMS m/z 210 (M+1), 233 (M+23).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07202248B2 |
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| Quelldatensatz | uspto-grants-2007_04 |
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| ORD ID | ord-23e5727e0f334e34a931020d1805252b |
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| Quellennotiz | uspto-grants-2007_04 |
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