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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25643Erstellt: 25. Oktober 2026

Ammonium Chloride → HCID 178486034, Verbindung

https://huagongshe.com/reaction/25643

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Edukt2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
EduktButyllithiumHCID 178418339—
EduktHCID 178486027HCID 178486027—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178486034HCID 178486034—

Reaktionsschritte

A solution of 10.0 g (25.2 mmol) of trans-[4-(2,2-Dibromo-vinyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester in 400 ml THF was treated at −78° C. with 33.0 ml (68.3 mmol) of BuLi (ca 1.6 M in hexane) and stirred for 2 h, then 27.8 ml (230.4 mmol) of DMPU were added and 10 min later 19.0 ml (125.9 mmol) of 2-(2-bromoethoxy)tetrahydro-2H-pyran dissolved in 20 ml were dropped in during 20 min. The reaction was warmed up to RT and stirred over night (approx. 16 h). An aqueous solution of saturated NH4Cl was added and the mixture was extracted with ether (3×). The organic phase was washed with H2O (2×), aqueous 10% NaCl and dried with Na2SO4, filtered and evaporated to give after flash column chromatography on silica gel (Hexane/EtOAc 19:1 to 3:1) 3.5 g (38%) of trans-Methyl-{4-[4-(tetrahydro-pyran-2-yloxy)-but-1-ynyl]-cyclohexyl}-carbamic acid tert-butyl ester, MS: 366 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858651B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-3434bbfe2c2a499c9641e5a0424417c2
Quellennotizuspto-grants-2005_02