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Diisobutylaluminum hydride → HCID 58700552, 화합물

HRID 517370
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HRID 517370 반응식
[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][C@@H:8]1[CH2:16][C@@H:11]2[O:12][C:13](=[O:15])[CH2:14][C@@H:10]2[C@H:9]1/[CH:17]=[CH:18]/[C@@H:19]([O:32][CH:33]1[CH2:38][CH2:37][CH2:36][CH2:35][O:34]1)[CH2:20][O:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([C:28]([F:31])([F:30])[F:29])[CH:23]=1.CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][C@@H:8]1[CH2:16][C@@H:11]2[O:12][CH:13]([OH:15])[CH2:14][C@@H:10]2[C@H:9]1/[CH:17]=[CH:18]/[C@@H:19]([O:32][CH:33]1[CH2:38][CH2:37][CH2:36][CH2:35][O:34]1)[CH2:20][O:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([C:28]([F:29])([F:30])[F:31])[CH:23]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 117874872HCID 117874872, 화합물

생성물 1

HCID 58700552HCID 58700552, 화합물수율 130.5%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
-70 °C

실험 절차

(3aR,4R,5R,6aS)-5-((tetrahydro-2H-pyran-2-yl)oxy)-4-((3R,E)-3-((tetrahydro-2H-pyran-2-yl)oxy)-4-(3-(trifluoromethyl)phenoxy)but-1-en-1-yl)hexahydro-2H-cyclopenta[b]furan-2-one (19.0 g, 35.3 mmol) was dissolved in toluene (200 mL), followed by cooling to −70° C., and DIBAL (1.0M in hexane, 53 mL, 53 mmol) was added dropwisely. Then the reaction was quenched by adding saturated aqueous solution of ammonium chloride (10 mL) at −70° C. The resulting mixture was poured into a 2M sodium bisulfate aqueous solution (200 mL) at room temperature and stirring was continued for 30 minutes. After separation of the organic layers, toluene (200 mL) was added to the aqueous layer. The combined organic layers were concentrated under reduced pressure to give 25.0 g of crude titled compound.

후처리

  1. customThen the reaction was quenched
  2. additionby adding saturated aqueous solution of ammonium chloride (10 mL) at −70° C
  3. additionThe resulting mixture was poured into a 2M sodium bisulfate aqueous solution (200 mL) at room temperature
  4. customAfter separation of the organic layers, toluene (200 mL)
  5. additionwas added to the aqueous layer
  6. concentrationThe combined organic layers were concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-57153dc46c514f20a3b754503ace30db
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115109B2

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