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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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[(2R,4R)-2-(4-methoxyphenyl)-5,5-dimethyl-1,3-dioxan-4-yl]methyl 4-nitrobenzoate → (2R)-2,4-dihydroxy-3,3-dimethylbutyl 4-nitrobenzoate

HRID 1643421
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HRID 1643421 반응식
[N+:1]([C:4]1[CH:29]=[CH:28][C:7]([C:8]([O:10][CH2:11][C@H:12]2[C:17]([CH3:19])([CH3:18])[CH2:16][O:15][C@@H](C3C=CC(OC)=CC=3)[O:13]2)=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2]>C1COCC1.C(O)(=O)C>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([C:8]([O:10][CH2:11][C@H:12]([OH:13])[C:17]([CH3:18])([CH3:19])[CH2:16][OH:15])=[O:9])=[CH:28][CH:29]=1)([O-:3])=[O:2]
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참가 물질

4

반응물 1

HCID 66754235[(2R,4R)-2-(4-methoxyphenyl)-5,5-dimethyl-1,3-dioxan-4-yl]methyl 4-nitrobenzoate

생성물 1

HCID 66753335(2R)-2,4-dihydroxy-3,3-dimethylbutyl 4-nitrobenzoate

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of compound obtained in Step C (4.4 g, 10.96 mmol) in THF (5 ml) and acetic acid (70%) (50 ml) was heated at 60° C. for 4 hours. The solvent was concentrated under reduced pressure and dissolved in EtOAc. The organic layer was washed with NaHCO3 and brine. The organic phase was concentrated under reduced pressure and the crude was crystallized from Et2O and n-Hexane at 0° C. to give a white solid.

후처리

  1. concentrationThe solvent was concentrated under reduced pressure
  2. dissolutiondissolved in EtOAc
  3. washThe organic layer was washed with NaHCO3 and brine
  4. concentrationThe organic phase was concentrated under reduced pressure
  5. customthe crude was crystallized from Et2O and n-Hexane at 0° C.
  6. customto give a white solid

출처 및 근거

ORD 기록
ord-f5d71b04f32b45f392452f615057f16e
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08119806B2

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