Methanol → 7-(3-Methoxy-5-oxocyclopent-1-EN-1-YL)heptanoic acid

HRID 461260

反応式

HRID 461260 の反応式
Br[CH:2]1[CH2:6][C:5](=[O:7])[C:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:3]1.N1C(C)=CC=CC=1C.[CH3:25][OH:26]>[B-](F)(F)(F)F.[Ag+]>[CH3:25][O:26][CH:2]1[CH2:6][C:5](=[O:7])[C:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:3]1

参加物

5

実験手順

To a stirred solution of 5.30 g. of crude 4-bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-one (Example 93) in 85 ml. of methanol at 0°-3° C. is added 4.40 g. (22.6 mmole) of silver fluoborate in one portion. After 2 minutes, the mixture is treated with 2.66 g. (24.8 mmoles) of 2,6-lutidine. After stirring for 30 minutes at 0°-3° C. the mixture is stirred at ambient temperature for 45 minutes. Silver bromide is removed by filtration, and the filtrate is concentrated to a volume of 40 ml. The solution is treated with saturated sodium chloride solution and extracted with ether. The extract is washed successively with 0.5N hydrochloric acid solution, water, and saturated sodium chloride solution; dried over magnesium sulfate; and concentrated. Partition chromatography of the residue on Celite gives an oil, λ maxMeOH. = 220 mμ (7450); ν max - 1715 (carbonyl groups) and 1095 cm-1 (methoxy group).

後処理

  1. additionthe mixture is treated with 2.66 g
  2. stirringis stirred at ambient temperature for 45 minutes
  3. customSilver bromide is removed by filtration
  4. concentrationthe filtrate is concentrated to a volume of 40 ml
  5. additionThe solution is treated with saturated sodium chloride solution
  6. extractionextracted with ether
  7. washThe extract is washed successively with 0.5N hydrochloric acid solution, water, and saturated sodium chloride solution
  8. dry with materialdried over magnesium sulfate
  9. concentrationand concentrated
  10. customPartition chromatography of the residue on Celite
  11. customgives an oil, λ maxMeOH

出典と根拠

ORDレコード
ord-ef54f193d2174bdeab23677e56e0f83d
出典データセット
uspto-grants-1977_12
特許番号
US04061672

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