o-Cyclohexylphenol → 3-Pyridinecarboxylic acid, 2-cyclohexylphenyl ester, hydrochloride

HRID 2413858

反応式

HRID 2413858 の反応式
[CH:1]1([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[OH:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.[C:15]([Cl:23])(=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=1>N1C=CC=CC=1>[ClH:23].[C:15]([O:13][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[CH:1]1[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1)(=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][CH:17]=1

参加物

4

反応物 2

HCID 8396o-CyclohexylphenolHCID 884383-Pyridinecarbonyl chloride, hydrochloride (1:1)

生成物 1

HCID 30596433-Pyridinecarboxylic acid, 2-cyclohexylphenyl ester, hydrochloride

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
30 °C

実験手順

15 g (85 mmol) of o-cyclohexylphenol and 16.5 g (93 mmol) of nicotinic acid chloride hydrochloride was mixed with 200 ml of dry pyridine and stirred for 24 hours at 30° C. After cooling precipitated pyridine hydrochloride was sucked off and 300 ml of water added. The precipitated raw product was washed with two 200 ml portions of water, dissolved in alcohol and reduced by means of a rotary evaporator. The remaining viscous oil was dissolved in 500 ml of dry ether and hydrochlorinated with HCl gas. Subsequently, the mixture was filtered, washed with ether and dried.

後処理

  1. temperatureAfter cooling
  2. customprecipitated pyridine hydrochloride
  3. addition300 ml of water added
  4. customThe precipitated raw product
  5. washwas washed with two 200 ml portions of water
  6. dissolutiondissolved in alcohol
  7. customreduced by means of a rotary evaporator
  8. dissolutionThe remaining viscous oil was dissolved in 500 ml of dry ether and hydrochlorinated with HCl gas
  9. filtrationSubsequently, the mixture was filtered
  10. washwashed with ether
  11. customdried

出典と根拠

ORDレコード
ord-af0c31276892453c901c210bb3fab831
出典データセット
uspto-grants-1988_01
特許番号
USRE032581

関連ノート

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