HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219612Erstellt: 24. Oktober 2026
HCID 88542676, Verbindung → tert-butyl (S)-1-(4-bromophenyl)ethyl((S)-4-((R)-1,1-dimethylethylsulfinamido)-6-methyl-4-phenylhept-6-enyl)carbamate
https://huagongshe.com/de/reaction/219612
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | HCID 88542676 | HCID 88542676 | — |
| Edukt | HCID 178448200 | HCID 178448200 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | tert-butyl (S)-1-(4-bromophenyl)ethyl((S)-4-((R)-1,1-dimethylethylsulfinamido)-6-methyl-4-phenylhept-6-enyl)carbamate | HCID 67986476 | — |
Reaktionsschritte
A solution of tert-butyl (S)-1-(4-bromophenyl)ethyl((E)-4-((R)-tert-butylsulfinylimino)-4-phenylbutyl)carbamate (1.97 g, 3.59 mmol) in dry THF (60 mL) was cooled to −78° C. A solution of 2-methylallylmagnesium chloride (0.5M in THF, 14.4 mL, 2 equiv) was added slowly. After 2 h, the mixture was warmed to rt and stirred for 1 h. LC-MS found reaction completed. The mixture was quenched with satd aq NH4Cl (10 mL), diluted with ether (100 mL), washed with water (30 mL), brine (25 mL), dried over Na2SO4. Filtration and concentration gave crude tert-butyl (S)-1-(4-bromophenyl)ethyl((S)-4-((R)-1,1-dimethylethylsulfinamido)-6-methyl-4-phenylhept-6-enyl)carbamate (2.30 g) which was used for next steps without further purifications. LC-MS Method 1 tR=2.53 min, m/z 605, 607(M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08202857B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-c8aff95c99b042608a1ab693a9689c76 |
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| Quellennotiz | uspto-grants-2012_06 |
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