تفاعل #6582

ord-4abdcb5f4ce64f6f9dc993a5b72d5eb7

معادلة التفاعل

OCCC12CC3CC(CC(C3)C1)C2
2-(1-adamantyl)ethanol
CCN(C(C)C)C(C)C
diisopropylethylamine
CCCCc1ncc(COC(C)=O)n1C(C)=O
1-acetyl-2-n-butyl 5-acetoxymethyl imidazole
O=S(=O)(OS(=O)(=O)C(F)(F)F)C(F)(F)F
triflic anhydride
CCCCc1ncc(COC(C)=O)n1CCC12CC3CC(CC(C3)C1)C2
5-acetoxymethyl-1-[2-(1-adamantyl)-ethyl]-2-n-butyl-imidazole

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated
  2. 2
    درجة الحرارةheated on a steam bath with 10% sodium hydroxide (250 ml)
  3. 3
    workup.ADDITIONdiluted with 300 ml of water
  4. 4
    استخلاصextracted with methylene chloride
  5. 5
    أخرىdried
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated
  8. 8
    أخرىto give an oil

الإجراء التجريبي

A mixture of 2-(1-adamantyl)ethanol (10.7 g) and diisopropylethylamine (11 ml) in methylene chloride (70 ml) was added to triflic anhydride (16.75 g) in 70 ml of methylene chloride at -78° C. for 45 minutes, 1-acetyl-2-n-butyl 5-acetoxymethyl imidazole in 50 ml of methylene chloride was added and the mixture was allowed to stand at room temperature for 4 days, then concentrated and heated on a steam bath with 10% sodium hydroxide (250 ml), diluted with 300 ml of water, extracted with methylene chloride, dried, filtered and concentrated to give an oil. Chromatography on silica gel in methanol/chloroform gave 5-acetoxymethyl-1-[2-(1-adamantyl)-ethyl]-2-n-butyl-imidazole. This acetoxy compound (5.4 g) was stirred at room temperature with potassium hydroxide (5.2 g) in ethanol (200 ml) for one hour, the mixture was concentrated, poured into water, stirred, and filtered to give 1-[2-(1-adamantyl)ethyl]-2-n-butyl-5-hydroxymethyl- 1H-imidazole.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05248689uspto-grants-1993_09