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Sodium Hydroxide → HCID 69311668, 화합물

HRID 33223
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HRID 33223 반응식
C[O:2][C:3](=[O:13])[CH2:4][CH2:5][CH2:6][CH:7]1[O:12][CH2:11][CH2:10][CH2:9][O:8]1.[OH-].[Na+]>O.CO>[O:8]1[CH2:9][CH2:10][CH2:11][O:12][CH:7]1[CH2:6][CH2:5][CH2:4][C:3]([OH:13])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 693128054-[1,3]Dioxan-2-yl-butyric acid methyl ester

생성물 1

HCID 69311668HCID 69311668, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

4-[1,3]Dioxan-2-yl-butyric acid methyl ester (6.8 g, 0.036 mol) was added to a stirred solution of sodium hydroxide (1.87 g, 0.047 mol) in water (30 ml) and methanol (30 ml). The mixture was stirred for 18 h at room temperature and then the solvent evaporated. The residue was partitioned between ethyl acetate (100 ml) and water (100 ml) and cooled to 0° C. The mixture was acidified with hydrochloric acid (1M) to pH 2 and the layers separated. The aqueous layer was further extracted with cold ethyl acetate (100 ml) and the combined organic layers washed with brine (100 ml) and then dried (Na2SO4). The solvents were evaporated and the crude solid (5.56 g) was used in the next step.

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후처리

  1. customthe solvent evaporated
  2. customThe residue was partitioned between ethyl acetate (100 ml) and water (100 ml)
  3. temperaturecooled to 0° C
  4. customthe layers separated
  5. extractionThe aqueous layer was further extracted with cold ethyl acetate (100 ml)
  6. washthe combined organic layers washed with brine (100 ml)
  7. dry with materialdried (Na2SO4)
  8. customThe solvents were evaporated

출처 및 근거

ORD 기록
ord-c63079a6f7f1435894ec7d9308a93c8f
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07429579B2

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