Reaktion #424901

ord-3fc117bbd9d64ddd9db3c5e6f0369bf5

Reaktionsgleichung

C1CCC2OC2CC1
1,2-epoxycycloheptane
Cn1cccn1
1-methylpyrazole
CN(C)CCN(C)C
N,N,N′,N′-tetramethylethylenediamine
[Li][CH2]CCC
n-butyl lithium
Cn1nccc1[C@H]1CCCCC[C@@H]1O
title compound
Ausbeute 13.0%
Cn1nccc1[C@H]1CCCCC[C@@H]1O
(1S*,2R*)-2-(1-Methyl-1H-pyrazol-5-yl)cycloheptanol
Ausbeute 13.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction and aftertreatment

Vorschrift

The reaction and aftertreatment were conducted in the same manner as in Example 4a by using 1-methylpyrazole (3.66 g, 44.6 mmol), N,N,N′,N′-tetramethylethylenediamine (6.68 mL, 44.6 mmol), n-butyl lithium (1.63 M solution in hexane; 32 mL, 52.2 mmol), 1,2-epoxycycloheptane (5.0 g, 44.6 mmol) and THF (60 mL), to yield the title compound (1.13 g, 13%) as a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08889741B2uspto-grants-2014_11