tert-Butanol → tert-Butyl (6-methoxynaphthalen-2-yl)carbamate

Reaktionsgleichung

[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8](C(O)=O)[CH:7]=[CH:6]2.C([N:18]([CH2:21]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:30])C=CC=CC=1.[C:40]([OH:44])([CH3:43])([CH3:42])[CH3:41]>>[C:40]([O:44][C:21](=[O:30])[NH:18][C:8]1[CH:7]=[CH:6][C:5]2[C:10](=[CH:11][CH:12]=[C:3]([O:2][CH3:1])[CH:4]=2)[CH:9]=1)([CH3:43])([CH3:42])[CH3:41]

Komponenten

Edukt 4

HCID 6386tert-Butanol

HCID 8471Triethylamine

HCID 199401P,P-Diphenylphosphinic azide

HCID 3491816-Methoxy-2-Naphthoic Acid

Produkt 1

HCID 57781067tert-Butyl (6-methoxynaphthalen-2-yl)carbamateAusbeute 82 %

Versuchsvorschrift

A mixture of 6-methoxy-naphthalene-2-carboxylic acid (10.00 g, 49.5 mmol), triethylamine (6.9 mL, 49.5 mmol) and diphenylphosphoryl azide (10.7 mL, 49.6 mmol) in 200 mL of anhydrous tert-butyl alcohol was refluxed under nitrogen for 5.5 h. The tert-butyl alcohol was removed under reduced pressure. The residue was dissolved in methylene chloride and extracted with 1 N HCl, 1 N NaOH, dried (MgSO4) and the solvent removed under reduced pressure to give (6-Methoxy-naphthalen-2-yl)-carbamic acid tert-butyl ester (11.14 g, 82%) as an off-white solid, mp 124-127° C.