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Methanol → (3S,3aR,6S,6aR)-hexahydrofuro[3,2-b]furan-3,6-diol

HRID 1676007
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HRID 1676007 반응식
C([O:9][C@H:10]1[CH2:14][O:13][C@@H:12]2[C@@H:15]([O:18]C(=O)C3C=CC=CC=3)[CH2:16][O:17][C@H:11]12)(=O)C1C=CC=CC=1.[OH-].[Na+].CO>O1CCCC1>[O:13]1[CH2:14][C@H:10]([OH:9])[C@H:11]2[O:17][CH2:16][C@H:15]([OH:18])[C@@H:12]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 11199023(3S,3aR,6S,6aR)-hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate

생성물 1

HCID 12304539(3S,3aR,6S,6aR)-hexahydrofuro[3,2-b]furan-3,6-diol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To (3S,3aR,6S,6aR)-hexahydrofuro[3,2-b]furan-3,6-diyl dibenzoate (6.30 g, 17.8 mmol), a mix of NaOH 10%:MeOH=1:1 (60 ml) was added. After stirring at room temperature for 24 hrs, the solvent was evaporated under reduced pressure. Water (30 ml) was added and extraction with EtOAc (30 ml) was carried out. The aqueous layer (pH adjusted to 6 with H3PO4 5%) was evaporated under reduced pressure to leave a white residue. Tetrahydrofuran was added in a large amount, then the suspension was filtered and the filtrate was concentrated to give the title product as a white solid.

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후처리

  1. customthe solvent was evaporated under reduced pressure
  2. additionWater (30 ml) was added
  3. extractionextraction with EtOAc (30 ml)
  4. customwas evaporated under reduced pressure
  5. customto leave a white residue
  6. filtrationthe suspension was filtered
  7. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-c82ede661d8f40c99a06aa15a981fdb5
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003811B2

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