تفاعل #1702074

ord-935790ee94ee465794ffa077fa2f1050

معادلة التفاعل

CC1(C)CCC(C)(C)c2cc3c(=O)ccoc3cc21
6,7,8,9-tetrahydro-6,6,9,9-tetramethyl-4H-naphtho[2,3-b]pyran-4-one
CC1(C)CCC(C)(C)c2cc3c(=O)ccoc3cc21
compound N
CC1(C)CCC(C)(C)c2cc3c(=O)ccoc3cc21
6,7,8,9-tetrahydro-6,6,9,9-tetramethyl-4H-naphtho[2,3-b]pyran-4-one
CO
methanol
CC1(C)CCC(C)(C)c2cc3c(cc21)OCCC3=O
2,3,6,7,8,9-hexahydro-6,6,9,9-tetramethyl-4H-naphtho[2,3-b]pyran-4-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe reaction solution was filtrated by celite
  2. 2
    تركيزthe filtrate was concentrated under reduced pressure
  3. 3
    أخرىThe crude product was purified by silica gel chromatography

الإجراء التجريبي

The synthesis process is as set forth in the chemical reaction formula below. To 6,7,8,9-tetrahydro-6,6,9,9-tetramethyl-4H-naphtho[2,3-b]pyran-4-one (the above named compound N) (124 mg, 0.48 mmol) were added methanol (4.0 mL), ethyl acetate (4.0 mL) and 10% palladium on carbon (40 mg), followed by stirring under a hydrogen atmosphere at room temperature for 10 hours. The reaction solution was filtrated by celite, and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel chromatography using hexane/ethyl acetate (4/1 to 2/1) as an elution solvent. The yield was 80.0 mg (64%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08765719B2uspto-grants-2014_07