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Hydrochloric Acid → HCID 178448086、化合物

HRID 2199024
ノート
印刷プレビュー

反応式

HRID 2199024 の反応式
[CH2:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]([C:10](O)=[O:11])[CH2:6][CH2:5]1)[CH2:2][CH3:3].[H-].[H-].[H-].[H-].[Li+].[Al+3].O.Cl>CCOCC>[CH2:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]([CH2:10][OH:11])[CH2:6][CH2:5]1)[CH2:2][CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 21226445Aluminium lithium hydride2 回HCID 178448101HCID 178448101、化合物

生成物 1

HCID 178448086HCID 178448086、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

このページの内容参加物実験手順後処理出典と根拠反応ノート

Trans-4-n-propylcyclohexane carboxylic acid (23.8 g, 0.14 mole), was dissolved in 150 ml of dry ether and added dropwise with stirring into a suspension of 11.4 g (0.3 mole) of LiAlH4 in 300 ml of ether. After the addition the mixture was heated for 2 hours at reflux, and then the supernatant LiAlH4 was decomposed with water while being cooled. The reaction mixture was then poured onto 20% hydrochloric acid and stirred until the inorganic salts dissolved. The product of formula (31) was extracted with diethyl ether; the combined organic phases were washed with water, dried with MgSO4 and concentrated.

後処理

  1. additionadded dropwise
  2. additionAfter the addition the mixture
  3. temperaturewas heated for 2 hours
  4. temperatureat reflux
  5. temperaturewhile being cooled
  6. dissolutiondissolved
  7. extractionThe product of formula (31) was extracted with diethyl ether
  8. washthe combined organic phases were washed with water
  9. dry with materialdried with MgSO4
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-dbc36f0d8f3145cc9f8c473ce4f463e0
出典データセット
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04361494

反応ノート

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