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Acetic Acid → (8-Fluoro-2,3-dihydro-1,4-benzodioxin-6-yl)methanol

HRID 253302
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HRID 253302 반응식
[F:1][C:2]1[C:7]2[O:8][CH2:9][CH2:10][O:11][C:6]=2[CH:5]=[C:4]([CH:12]=[O:13])[CH:3]=1.[BH4-].[Na+].C(O)(=O)C>C(O)C>[F:1][C:2]1[C:7]2[O:8][CH2:9][CH2:10][O:11][C:6]=2[CH:5]=[C:4]([CH2:12][OH:13])[CH:3]=1
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참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 4311764Sodium borohydrideHCID 574231098-Fluoro-2,3-dihydro-1,4-benzodioxin-6-carboxaldehyde

생성물 1

HCID 66891073(8-Fluoro-2,3-dihydro-1,4-benzodioxin-6-yl)methanol수율 95%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

8-fluoro-2,3-dihydro-1,4-benzodioxine-6-carbaldehyde (0.87 g: 4.8 mmol) was dissolved in ethanol (20 ml) and sodium borohydride (0.45 g; 11.95 mmol) was added at 0° C. The reaction mixture was stirred at rt for 2 h and poured into ice-water. The pH was adjusted to 5 by adding glacial acetic acid in portions and the aqueous mixture was extracted with ethyl acetate (80 ml). The organic phase was washed with water (30 ml), brine (30 ml), dried over sodium sulfate and concentrated under vacuum to give (8-fluoro-2,3-dihydro-1,4-benzodioxin-6-yl)methanol (0.84 g; 95% yield) as a yellow oil. 1H NMR (400 MHz, CD3OD) δ 6.66 (dd, 1H), 6.64 (br. s, 1H), 4.44 (s, 2H), 4.26 (s, 4H)

후처리

  1. extractionthe aqueous mixture was extracted with ethyl acetate (80 ml)
  2. washThe organic phase was washed with water (30 ml), brine (30 ml)
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-9bfda7ac9c7a436ca5f8bc9452f80996
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07872014B2

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