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Hydrochloric Acid → 2-(Dimethylaminophenylmethyl)cyclohexanol

HRID 459662
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HRID 459662 반응식
[BH4-].[Na+].[CH3:3][N:4]([CH:6]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][C:8]1=[O:13])[CH3:5].Cl>CO>[CH3:5][N:4]([CH:6]([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[OH:13])[CH3:3]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 4311764Sodium borohydrideHCID 111722992-(Dimethylaminophenylmethyl)cyclohexanone

생성물 1

HCID 112647962-(Dimethylaminophenylmethyl)cyclohexanol수율 94%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A total of 28.3 g (747 mmole) sodium borohydride, dissolved in 650 ml methanol, were added in portions to 80.0 g (299 mmole) of the 2-(dimethylaminophenylmethyl)cyclohexanone prepared according to Example 1 (2nd stage), and the mixture was subsequently stirred for one hour. For working up, 680 ml dilute hydrochloric acid (1 N) were added, and the mixture was extracted with 500 ml ether. The aqueous phase was rendered alkaline (pH≧10) with 25 vol. % ammonia solution and extracted three times with 250 ml ether each time. The combined organic extracts were dried over sodium sulfate, filtered and concentrated on a rotary evaporator (500 to 10 mbar). 65.2 g (94% of theoretical) 2-(dimethylaminophenylmethyl)cyclohexanol were obtained.

후처리

  1. customprepared
  2. extractionthe mixture was extracted with 500 ml ether
  3. extractionextracted three times with 250 ml ether each time
  4. dry with materialThe combined organic extracts were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated on a rotary evaporator (500 to 10 mbar)

출처 및 근거

ORD 기록
ord-d3a718bff7e243cca1067990bc07c61a
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE039530E1

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