Cyclobutanecarboxylic acid, 3-ethyl- → 1-(3-Ethylcyclobutyl)ethanone

HRID 1680731

反応式

HRID 1680731 の反応式
[CH2:1]([CH:3]1[CH2:6][CH:5]([C:7]([OH:9])=O)[CH2:4]1)[CH3:2].[CH3:10][Li]>CCOCC>[C:7]([CH:5]1[CH2:4][CH:3]([CH2:1][CH3:2])[CH2:6]1)(=[O:9])[CH3:10]

参加物

4

実験手順

A solution of 6.61 g of 3-ethylcyclobutane-1-carboxylic acid, in 52 ml of distilled ether was stirred under argon at 0°. Methyllithium (85.0 ml of a 1.53 M solution in ether) was added dropwise over a 30 minute period. The reaction mixture was stirred for three hours at 25°, then quenched with 7.3 water-methanol. The layers were separated, and the aqueous layer extracted with ether. The combined organic layers were washed with brine, dried, filtered and the solvents evaporated in vacuo. The resultant oil was distilled (aspirator vacuum) to afford 5.5 g of 1-acetyl-3-ethylcyclobutane, as a clear oil (bp 64°-67°). The material had the following spectral characteristics: nmr (CDCl3) δ 0.80 and 0.82 (3H total, pair of t, each J=7.0 Hz), 1.10 and 1.12 (ca. 1.5H total, pair of s, side product 1-[2-hydroxy-prop-2-yl]-3-ethylcyclobutane), 1.0-2.4 (7 H, m), 2.07 and 2.09 (3H total, pair of s) and 2.7-3.5 ppm (1H, m); ir (CHCl3) 935, 1175, 1370, 1460, 1705, 2870, 2930 and 2970 cm-1, also small 3200-3600 broad and 3600 cm-1 for the side product noted above.

後処理

  1. customquenched with 7.3 water-methanol
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted with ether
  4. washThe combined organic layers were washed with brine
  5. customdried
  6. filtrationfiltered
  7. customthe solvents evaporated in vacuo
  8. distillationThe resultant oil was distilled (aspirator vacuum)

出典と根拠

ORDレコード
ord-d455ee066f7f494084a5e26a1c625507
出典データセット
uspto-grants-1981_06
特許番号
US04275224

関連ノート

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