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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Heptanethiol → HCID 85639082, 화합물

HRID 2226475
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HRID 2226475 반응식
[O-]CC.[Na+].[Na].Cl.[Cl:7][CH2:8][CH2:9][N:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1.[CH2:16]([SH:23])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]>C(O)C>[ClH:7].[CH2:16]([S:23][CH2:8][CH2:9][N:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]
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참가 물질

6

반응물 4

HCID 154221-HeptanethiolHCID 74826Piperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 2723922Sodium ethoxide3회HCID 5360545Sodium

생성물 1

HCID 85639082HCID 85639082, 화합물수율 83.3%

시약·촉매·용매 1

HCID 702Ethanol용매3회

실험 절차

Generate sodium ethoxide by carefully adding sodium metal (1.4 g, 60 mmol) to absolute ethanol (50 mL). Add 1/2 of the sodium ethoxide (30 mL) to a solution of N-(2-chloroethyl)-piperidine hydrochloride (5.0 g, 27.2 mmol) in absolute ethanol. Add the other 1/2 of the sodium ethoxide (30 mL) to a solution of heptyl mercaptan (4.6 mL, 30 mmol) in absolute ethanol. Mix the two and stir at room temperature overnight. Concentrate in vacuo, partition between water and ethyl acetate and separate the organic phase. Extract the aqueous phase with ethyl acetate (2×50 mL), combine the organic phases and dry (MgSO4). Evaporate the solvent in vacuo to yield 6.34 g yellow oil. Dissolve the oil in ethyl ether, filter and treat with anhydrous hydrochloric acid. Collect the resulting white solid by vacuum filtration (5.6 g) and recrystallize (ethyl acetate/isopropanol) to yield 3.12 g of the title compound as white crystals; mp 169°-70° C.

후처리

  1. additionMix the two
  2. concentrationConcentrate in vacuo
  3. custompartition between water and ethyl acetate
  4. customseparate the organic phase
  5. extractionExtract the aqueous phase with ethyl acetate (2×50 mL)
  6. dry with materialdry (MgSO4)
  7. customEvaporate the solvent in vacuo

출처 및 근거

ORD 기록
ord-0f118c7830f04177b07150c64c033331
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05348964

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