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Trimethylsilyldiazomethane → 3-(5-Methyl-2-phenyl-oxazol-4-yl)-propan-1-ol

HRID 2121694
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HRID 2121694 반응식
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][CH2:14][C:15](O)=[O:16].C[Si](C=[N+]=[N-])(C)C.[BH4-].[Na+]>CO.C1(C)C=CC=CC=1>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][CH2:14][CH2:15][OH:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 167693TrimethylsilyldiazomethaneHCID 4311764Sodium borohydrideHCID 120932643-(5-Methyl-2-phenyl-4-oxazolyl)propionic acid

생성물 1

HCID 120932653-(5-Methyl-2-phenyl-oxazol-4-yl)-propan-1-ol수율 71.3%

시약·촉매·용매 1

HCID 21867641Toluene methanol용매

실험 절차

Acid 1-3 (4.6 g, 20 mmol) was dissolved in 300 mL of a 1:1 mixture of methanol/toluene at 23° C. under N2 atmosphere. Trimethylsilyl diazomethane (20 mL, 40 mmol), added dropwise until color persisted and stirred for an additional 4 hours. Solvent was removed in vacuo and residue dried under vacuum for 1 hour. Residue was then redissolved in 300 mL methanol and placed under N2 atmosphere. NaBH4 (10 g, 264 mmol)and the reaction stirred for 4 hours. When complete, solvent was removed in vacuo and residue taken up in ethyl acetate and washed with water, brine and dried over MgSO4. SiO2 chromatography with 40% EtOAc/Hexanes gave 3.1 g of the product 1-4 as white crystals (71%) M.P. NMR CDCl3 (δ): 8.01 (2H, m); 7.44 (3H, m); 3.75 (2H, t, J=5.8, 11.4 Hz); 2.68 (2H, t, 6.8, 13.7 Hz); 2.35 (3H, s); 1.91 (2H, m).

후처리

  1. customSolvent was removed in vacuo and residue
  2. customdried under vacuum for 1 hour
  3. dissolutionResidue was then redissolved in 300 mL methanol
  4. customWhen complete, solvent was removed in vacuo and residue
  5. washwashed with water, brine
  6. dry with materialdried over MgSO4

출처 및 근거

ORD 기록
ord-9df11929481b4f5cb5390ac61388f07a
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06696474B2

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