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Hydrochloric Acid → HCID 178448086, 화합물

HRID 2199024
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HRID 2199024 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 21226445Aluminium lithium hydride2회HCID 178448101HCID 178448101, 화합물

생성물 1

HCID 178448086HCID 178448086, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

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.

후처리

  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

출처 및 근거

ORD 기록
ord-dbc36f0d8f3145cc9f8c473ce4f463e0
출처 데이터셋
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04361494

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