HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13010Erstellt: 23. Oktober 2026
Isopropanol → tert-Butyl ((1R,2S)-1-hydroxy-1-(3-methoxyphenyl)propan-2-yl)carbamate
https://huagongshe.com/de/reaction/13010
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | Aluminum isopropoxide | HCID 11143 | — |
| Edukt | tert-Butyl [(1S)-2-(3-methoxyphenyl)-1-methyl-2-oxoethyl]carbamate | HCID 59339682 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | tert-Butyl ((1R,2S)-1-hydroxy-1-(3-methoxyphenyl)propan-2-yl)carbamate | HCID 59339845 | 98,5% |
Reaktionsschritte
A mixture of tert-butyl[(1S)-2-(3-methoxyphenyl)-1-methyl-2-oxoethyl]carbamate (13.6 g, 48.7 mmol), aluminium isopropoxide (1.99 g, 9.70 mmol), 2-propanol (41 mL, 535 mmol) in toluene (63 mL) was stirred under an atmosphere of argon at 50° C. overnight. LC/MS showed complete conversion into the alcohol. The mixture was partitioned between ethyl acetate (200 mL) and hydrochloric acid (1M, 200 mL). The organic phase was washed with water (200 mL), dried over magnesium sulfate and concentrated to give the subtitle compound as a syrup (13.5 g). The compound was used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728030B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-3db14460337a45d2bea3c5845afb4297 |
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| Quellennotiz | uspto-grants-2010_06 |
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