Acetic Acid → (S)-2-ethynyl-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol

HRID 1199324

Reaktionsgleichung

C(O[C@@:5]([CH3:21])([C:19]#[CH:20])[CH2:6][CH2:7][C:8]1[C:9](=[O:18])[C:10]([CH3:17])=[C:11]([CH3:16])[C:12](=[O:15])[C:13]=1[CH3:14])(=O)C.C(O)(=O)C>C(Cl)Cl.[Zn]>[C:19]([C@:5]1([CH3:21])[CH2:6][CH2:7][C:8]2[C:13]([CH3:14])=[C:12]([OH:15])[C:11]([CH3:16])=[C:10]([CH3:17])[C:9]=2[O:18]1)#[CH:20]

Komponenten

Reaktionsbedingungen

Temperatur: 4 °C

Versuchsvorschrift

A solution of 285 mg (0.99 mmol) of (R)-2-[3-(acetyloxy)-3-methyl-4-pentynyl]-3,5,6-trimethyl-2,5-cyclohexadiene-1,4-dione in 4 mL of CH2Cl2 was stirred with 250 mg of Zn dust, and 250 mg of glacial acetic acid. The reaction mixture was stirred at 4° C. under argon for 50 min, then filtered. It was worked up with CH2Cl2 as described above. The crude hydroquinone acetate was taken into 6 mL of CH2Cl2 and treated with 20 mg of AgClO4.H2O as described above to give 124 mg of crude product after workup, and purification by flash chromatography. Crystallization of this material from toluene-hexane (1:1) at -15° C. gave 57 mg of (S)-2-ethynyl-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol: [α]D25 +20.20°, (c 1.3, CHCl3).

Aufarbeitung

filtrationfiltered
additiontreated with 20 mg of AgClO4.H2O
customto give 124 mg of crude product
customafter workup, and purification by flash chromatography
customCrystallization of this material from toluene-hexane (1:1) at -15° C.

Quellen und Nachweise

ORD-Eintrag: ord-0c59fb68e63f43c2abe00bca3c65ebfc
Quelldatensatz: uspto-grants-1990_02
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US04900476

Verknüpfte Notizen

Wird geladen…