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2-methylspiro[3.3]heptane-2-carboxylic acid → HCID 20320778、化合物

HRID 866395
ノート
印刷プレビュー

反応式

HRID 866395 の反応式
[CH3:1][C:2]1([C:9]([OH:11])=O)[CH2:5][C:4]2([CH2:8][CH2:7][CH2:6]2)[CH2:3]1.[CH3:12][Li]>CCOCC>[CH3:1][C:2]1([C:9](=[O:11])[CH3:12])[CH2:3][C:4]2([CH2:6][CH2:7][CH2:8]2)[CH2:5]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 203207772-methylspiro[3.3]heptane-2-carboxylic acidHCID 178418348HCID 178418348、化合物

生成物 1

HCID 20320778HCID 20320778、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
25 °C

実験手順

A solution of 5.0 g (33.0 mmol) 2-methylspiro[3.3]heptane-2-carboxylic acid in 33.0 ml of dry ether was stirred under argon at 0° C and 47.6 ml (74.3 mmol) of 1.56 M methyl lithium in ether added dropwise. The reaction mixture was allowed to warm to 25° C and was stirred for 3.0 hr. The reaction mixture was cooled to -20° C and quenched by addition of 10% aqueous HCl. The layers were separated and the aqueous layer extracted with ether. The combined organic layers were washed with saturated aqueous sodium bicarbonate and brine, then dried (MgSO4), filtered, and evaporated in vacuo to afford 2-methyl-2-acetylspiro[3.3]heptane as a light yellow oil (4.91 g 98%).

後処理

  1. temperatureThe reaction mixture was cooled to -20° C
  2. customquenched by addition of 10% aqueous HCl
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with ether
  5. washThe combined organic layers were washed with saturated aqueous sodium bicarbonate and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated in vacuo

出典と根拠

ORDレコード
ord-50122c90e0b540f0acefcad7db2d1dc0
出典データセット
uspto-grants-1978_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04098823

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート