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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 627177Erstellt: 26. Oktober 2026

Nitrogen → HCID 89852321, Verbindung

https://huagongshe.com/reaction/627177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktVinyloxiraneHCID 13586—
EduktTert-butyl N-(benzyloxy)carbamateHCID 736159—
KatalysatorTetrabutylammonium BromideHCID 74236—
KatalysatorPalladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 89852321HCID 8985232193%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

In a 3 L RBF, a solution of tert-butyl benzyloxycarbamate (Intermediate 153, 86.9 g, 389.22 mmol), N,N(1S,2S)-cyclohexane-1,2-diyl)bis(2-(diphenylphosphino)-1-naphthamide) (18.5 g, 23.39 mmol), Pd2(dba)3-CHCl3 (8.05 g, 7.78 mmol) and TBAB (150.5 g, 466.81 mmol) in acetonitrile (1.8 L) was bubbled with N2 for 30 minutes and the flask was closed with a rubber septum. The solution was then kept in a −20° C. freezer for 2 hrs. 2-vinyloxirane (30 g, 428.02 mmol, 1.10 equiv) was added and the mixture was stirred in the freezer (−20-25° C.) for 3 days. The mixture was filtered and the filtrate was evaporated. The residue was purified by silica gel column eluted with EtOAc/hexane (0-40%) to give the title compound (106 g, 93%) as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09309245B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-acb24115ddb249fe8edce1770a1d3d32
Quellennotizuspto-grants-2016_04