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

HRID 223573노트

반응식

HRID 223573 반응식
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

참가 물질

7

반응물 4

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

생성물 1

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

시약·촉매·용매 2

HCID 962Water용매HCID 3283Diethyl Ether용매

실험 절차

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.).

후처리

  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

출처 및 근거

ORD 기록
ord-0e4c24cfbbe5432fa658a10f1ef18a9e
출처 데이터셋
uspto-grants-1982_10
특허 번호
US04355037

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