홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

1-Octanethiol → 4-{1-[2-(4-Cyanophenyl)ethyl]-4-hydroxypiperidin-4-ylmethoxy}benzoic acid

HRID 1727094
노트
인쇄 미리보기

반응식

HRID 1727094 반응식
C(S)CCCCCCC.C([Li])CCC.[C:15]([C:17]1[CH:22]=[CH:21][C:20]([CH2:23][CH2:24][N:25]2[CH2:30][CH2:29][C:28]([CH2:32][O:33][C:34]3[CH:43]=[CH:42][C:37]([C:38]([O:40]C)=[O:39])=[CH:36][CH:35]=3)([OH:31])[CH2:27][CH2:26]2)=[CH:19][CH:18]=1)#[N:16]>CCCCCC.CN(C)P(=O)(N(C)C)N(C)C.O1CCCC1>[C:15]([C:17]1[CH:18]=[CH:19][C:20]([CH2:23][CH2:24][N:25]2[CH2:26][CH2:27][C:28]([CH2:32][O:33][C:34]3[CH:35]=[CH:36][C:37]([C:38]([OH:40])=[O:39])=[CH:42][CH:43]=3)([OH:31])[CH2:29][CH2:30]2)=[CH:21][CH:22]=1)#[N:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 81441-OctanethiolHCID 10157471Methyl 4-{1-[2-(4-cyanophenyl)ethyl]-4-hydroxypiperidin-4-ylmethoxy}benzoateHCID 178418339Butyllithium

생성물 1

HCID 101778054-{1-[2-(4-Cyanophenyl)ethyl]-4-hydroxypiperidin-4-ylmethoxy}benzoic acid수율 75.9%

시약·촉매·용매 3

HCID 8028Tetrahydrofuran용매2회
HCID 8058
Hexane
용매
HCID 12679Hexamethylphosphoramide용매2회

실험 절차

To a solution of n-octanethiol (2.04 g) in a mixture of anhydrous tetrahydrofuran (10 mL) and anhydrous hexamethylphosphoric triamide (HMPA) (5 mL), a 1.59 M solution of n-butyl lithium in hexane (8.74 mL) was added dropwise under cooling with ice-water under nitrogen atmosphere. After stirring at the same temperature for fifteen minutes, a solution of the compound (2.50 g) obtained in Example 13 in a mixture of anhydrous tetrahydrofuran (10 mL) and anhydrous HMPA (5 mL) was added dropwise thereto over ten minutes, followed by stirring at the same temperature for thirty minutes and further stirring at room temperature for seventeen hours. After the completion of reaction, the reaction mixture was mixed with an ice water (20 mL) under cooling with ice-water and was washed with ethyl acetate (25 mL×2). Small portions of 3 N hydrochloric acid were gradually added to the aqueous layer with stirring under cooling with ice-water, to adjust the pH of the mixture to 5.6. The precipitated crystals were collected by filtration and were sequentially washed with water and ethanol. The resulting crystals were suspended in a mixture of methanol (50 mL) and water (10 mL), followed by heating under reflux for thirty minutes. After standing to cool, the crystals were collected by filtration and were washed with methanol, and dried under reduced pressure to yield the titled compound (1.83 g) as crystals.

후처리

  1. additionwas added dropwise
  2. waitover ten minutes
  3. stirringby stirring at the same temperature for thirty minutes
  4. stirringfurther stirring at room temperature for seventeen hours
  5. customAfter the completion of reaction
  6. washwas washed with ethyl acetate (25 mL×2)
  7. additionSmall portions of 3 N hydrochloric acid were gradually added to the aqueous layer
  8. stirringwith stirring
  9. temperatureunder cooling with ice-water
  10. filtrationThe precipitated crystals were collected by filtration
  11. washwere sequentially washed with water and ethanol
  12. additionThe resulting crystals were suspended in a mixture of methanol (50 mL) and water (10 mL)
  13. temperatureby heating
  14. temperatureunder reflux for thirty minutes
  15. temperatureto cool
  16. filtrationthe crystals were collected by filtration
  17. washwere washed with methanol
  18. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-4c1fec0d97e7407eaf472f7393baa79f
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07494987B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트