HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 865465Erstellt: 26. Oktober 2026
Acetic Acid → 2-(S)-(Phenylmethylthiomethyl)butanoic Acid
https://huagongshe.com/reaction/865465
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Benzyl 2-(S)-(Phenylmethylthiomethyl)butanoate | HCID 9995793 | — |
| Lösungsmittel | Hydrogen Bromide | HCID 260 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-(S)-(Phenylmethylthiomethyl)butanoic Acid | HCID 10263053 | 76,2% |
Reaktionsschritte
Glacial HOAc (120 ml) was added to a suspension of the product of step 8 (32.4 g, approx. 103 mmol) in 210 ml of 30-32% anhydrous HBr in glacial HOAc (approx. 1.03 mol) to complete the dissolution. The resulting solution was stirred at 70° C. for 6h and at 50° overnight. The reaction mixture was then cooled to r.t., diluted with H2O (750 mL) and extracted with CH2Cl2 (7×). The combined organic extracts were concentrated in vacuo. The residue was diluted with toluene (500 mL) and concentrated in vacuo 5 times to remove HOAc. The residue was dissolved in 1M aq KOH (750 mL), washed with CH2Cl2 (4×), acidified to pH 1 with concentrated HCl and extracted with CH2Cl2 (6×). The combined organic extracts were dried over Na2SO4 and concentrated in vacuo to afford 17.6 g of the title compound as a pale yellow liquid which was used as such for the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05565473 |
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| Quelldatensatz | uspto-grants-1996_10 |
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| ORD ID | ord-19fb5ecaeac7493f99684ceaf399c700 |
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| Quellennotiz | uspto-grants-1996_10 |
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