HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25654Erstellt: 24. Oktober 2026
Sodium Thiosulfate → Benzyl methyl4-oxocyclohexylcarbamate
https://huagongshe.com/de/reaction/25654
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Thiosulfate | HCID 24477 | — |
| Edukt | Potassium Bromide | HCID 253877 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium Hypochlorite | HCID 23665760 | — |
| Edukt | HCID 178485997 | HCID 178485997 | — |
| Katalysator | Tempo | HCID 2724126 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Benzyl methyl4-oxocyclohexylcarbamate | HCID 58562802 | 99% |
Reaktionsschritte
A solution of 2.63 g (10 mmol) of cis-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid benzyl ester in 16 ml CH2Cl2 was treated with a solution 0.24 g (2 mmol) of KBr and 0.28 g (3.33 mmol) of NaHCO3 in 5 ml of water. The suspension was cooled (0-5° C.) and 8 mg (0.05 mmol) of TEMPO and then 5.7 ml (12.5 mmol) of NaOCl (13%, 2.18 M in water) were added during 20 min. After 1 h at this temperature, again 8 mg (0.05 mmol) of TEMPO and then 2.85 ml (6.25 mmol) of NaOCl (13%, 2.18 M in water) were added. After 1 h, 5 ml of 1M sodium thiosulfat solution was added. The aqueous phase was extracted with CH2Cl2(2×), the organic phase was dried (Na2SO4), filtered and evaporated to give 2.57 g (99%) of Methyl-(4-oxo-cyclohexyl)-carbamic acid benzyl ester, MS: 261 (M).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06858651B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-684046808ff74118b5c422a3a65be5d6 |
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| Quellennotiz | uspto-grants-2005_02 |
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