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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1199324Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1199324

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt(R)-2-[3-(acetyloxy) 3-methyl-4-pentynyl]-3,5,6-trimethyl-2,5-cyclohexadiene-1,4-dioneHCID 14478578—
KatalysatorZincHCID 23994—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-2-ethynyl-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-6-olHCID 985944025%

Reaktionsbedingungen

Temperatur4 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04900476
Quelldatensatzuspto-grants-1990_02
ORD IDord-0c59fb68e63f43c2abe00bca3c65ebfc
Quellennotizuspto-grants-1990_02