Hydrochloric Acid → 3-(4-Piperidinyl)-1,2-benzisoxazole Hydrochloride

HRID 647298ノート

反応式

HRID 647298 の反応式
C1(OC([N:10]2[CH2:15][CH2:14][CH:13]([C:16]3[C:20]4[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=4[O:18][N:17]=3)[CH2:12][CH2:11]2)=O)C=CC=CC=1.C(O)C.[OH-].[K+].[ClH:30]>CCOCC.O>[ClH:30].[NH:10]1[CH2:11][CH2:12][CH:13]([C:16]2[C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=3[O:18][N:17]=2)[CH2:14][CH2:15]1

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 14797Potassium HydroxideHCID 13076435Phenyl 4-(1,2-benzoxazol-3-yl)piperidine-1-carboxylate

生成物 1

HCID 130764373-(4-Piperidinyl)-1,2-benzisoxazole Hydrochloride収率 57%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 3283Diethyl Ether溶媒

実験手順

A mixture of 5.0 g of 4-(1,2-benzisoxazole-3-yl)-1-piperidine carboxylic acid phenyl ester, 100 ml of ethanol, 50 g of (85%) potassium hydroxide and 50 ml of water was heated under reflux, with stirring, under nitrogen for 16 hrs. Most of the ethanol was removed in vacuo and the resultant aqueous suspension was extracted with ether (3×50 ml). The ether extracts were combined, washed with water, dried over anhydrous magnesium sulfate and the ether removed under reduced pressure to give an oil. The oil was dissolved in anhydrous ether and hydrogen chloride was introduced to precipitate a 3.0 g of a hydrochloride salt. Recrystallization from methanol-ether gave 2.0 g (57%) of product as the hydrochloride, mp, 313°-315° (dec.).

後処理

  1. temperaturewas heated
  2. temperatureunder reflux
  3. customMost of the ethanol was removed in vacuo
  4. extractionthe resultant aqueous suspension was extracted with ether (3×50 ml)
  5. washwashed with water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe ether removed under reduced pressure
  8. customto give an oil
  9. customto precipitate a 3.0 g of a hydrochloride salt
  10. customRecrystallization from methanol-ether

出典と根拠

ORDレコード
ord-9ae401f9710746528de10b1766c0bfe0
出典データセット
uspto-grants-1983_10
特許番号
US04408053

反応ノート

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