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Propyl mercaptan → N-(2-Propenyl)-cis-2-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-4-piperidinol

HRID 371160
ノート
印刷プレビュー

反応式

HRID 371160 の反応式
C(S)CC.C([Li])CCC.[CH2:10]([N:13]1[CH2:18][CH2:17][C@H:16]([OH:19])[CH2:15][C@@H:14]1[C:20]1[CH:25]=[CH:24][C:23]([C:26]([CH3:34])([CH3:33])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:22][C:21]=1[O:35]CC1C=CC=CC=1)[CH:11]=[CH2:12].C([S-])CC.[Li+]>O1CCCC1.CCCCCC.CN(C)P(N(C)C)(N(C)C)=O>[CH2:10]([N:13]1[CH2:18][CH2:17][C@H:16]([OH:19])[CH2:15][C@@H:14]1[C:20]1[CH:25]=[CH:24][C:23]([C:26]([CH3:34])([CH3:33])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[CH:22][C:21]=1[OH:35])[CH:11]=[CH2:12]
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

8

反応物 4

HCID 7848Propyl mercaptanHCID 10909481Lithium propanethiolateHCID 70490735N-(2-Propenyl)-cis-2-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidinolHCID 178418339Butyllithium

生成物 1

HCID 70491522N-(2-Propenyl)-cis-2-[4-(1,1-dimethylheptyl)-2-hydroxyphenyl]-4-piperidinol収率 58%

試薬・触媒・溶媒 3

HCID 8028
Tetrahydrofuran
溶媒
HCID 8058Hexane溶媒
HCID 12679Hexamethylphosphoramide溶媒

反応条件

温度
25 °C

実験手順

A solution of 6.8 ml (74.6 mmole) of propanethiol in 75 ml of tetrahydrofuran is degassed by three freeze-thaw cycles at 0.1 torr. The resultant solution is cooled to -78° C. and 28 ml of 2.5M n-butyllithium in hexane is added. The reaction is then allowed to warm to 25° C. and stirred 3 hours longer. The reaction is evaporated to dryness under high vacuum and the residue dissolved in 70 ml of degassed hexamethylphosphoramide. To a 25° C. degassed solution of 218 mg (0.486 mmole) of N-(2-propenyl)-cis-2-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidinol in 1 ml of hexamethylphosphoramide is added 2.2 ml of the above prepared solution of lithium propanethiolate. The reaction is stirred 30 minutes at 25° C. and 1.5 hour at 105° C. followed by cooling to 25° C. The reaction is quenched by addition to 30 ml water and the mixture extracted with 150 ml ethyl ether. The ether extract is washed twice with 30 ml water, once with 30 ml saturated sodium chloride, dried over magnesium sulfate and evaporated to an oil. The crude product is purified via column chromatography on 48 g of silica gel eluting in 8 ml fractions with ethyl ether to give (fractions 12-24) 101 mg (58%) of the title compound as an oil.

後処理

  1. customThe reaction is evaporated to dryness under high vacuum
  2. dissolutionthe residue dissolved in 70 ml of degassed hexamethylphosphoramide
  3. stirringThe reaction is stirred 30 minutes at 25° C. and 1.5 hour at 105° C.
  4. temperatureby cooling to 25° C
  5. customThe reaction is quenched by addition to 30 ml water
  6. extractionthe mixture extracted with 150 ml ethyl ether
  7. extractionThe ether extract
  8. washis washed twice with 30 ml water, once with 30 ml saturated sodium chloride
  9. dry with materialdried over magnesium sulfate
  10. customevaporated to an oil
  11. customThe crude product is purified via column chromatography on 48 g of silica gel eluting in 8 ml fractions with ethyl ether

出典と根拠

ORDレコード
ord-ba3bf8426ac3456f956aad9db66b5dc6
出典データセット
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04529732

反応ノート

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