반응 #1702074

ord-935790ee94ee465794ffa077fa2f1050

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The reaction solution was filtrated by celite
  2. 2
    농축the filtrate was concentrated under reduced pressure
  3. 3
    기타The crude product was purified by silica gel chromatography

실험 절차

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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08765719B2uspto-grants-2014_07