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Iodoethane → Ethyl 5-(ethoxymethyl)-4,5-dihydroisoxazole-3-carboxylate

HRID 58540
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HRID 58540 반응식
[H-].[Na+].[OH:3][CH2:4][CH:5]1[O:9][N:8]=[C:7]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH2:6]1.I[CH2:16][CH3:17]>CN(C=O)C>[CH2:16]([O:3][CH2:4][CH:5]1[O:9][N:8]=[C:7]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH2:6]1)[CH3:17]
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참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 23643400Ethyl 5-(hydroxymethyl)-4,5-dihydro-1,2-oxazole-3-carboxylate

생성물 1

HCID 66831765Ethyl 5-(ethoxymethyl)-4,5-dihydroisoxazole-3-carboxylate수율 40.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Sodium hydride (0.141 g; 3.51 mmol) was added to a solution of ethyl 5-(hydroxymethyl)-4,5-dihydroisoxazole-3-carboxylate (0.338 g; 1.76 mmol) in DMF (3 mL) in an ice bath. The mixture was stirred for 10 min before addition of iodoethane (0.430 mL; 5.27 mmol). The ice bath was removed and the mixture was stirred at room temperature for 2 h. After evaporation, the residue was partitioned between brine and dichloromethane and the solution extracted with dichloromethane. Organic extracts were evaporated and the residue was purified by flash chromatography on silica gel (eluent: 1-6% ethyl acetate in dichloromethane) to afford 0.142 g (40%) of ethyl 5-(ethoxymethyl)-4,5-dihydroisoxazole-3-carboxylate.

후처리

  1. customThe ice bath was removed
  2. customAfter evaporation
  3. customthe residue was partitioned between brine and dichloromethane
  4. extractionthe solution extracted with dichloromethane
  5. customOrganic extracts were evaporated
  6. customthe residue was purified by flash chromatography on silica gel (eluent: 1-6% ethyl acetate in dichloromethane)

출처 및 근거

ORD 기록
ord-c02caa71ff834a129605d4fc49a44f1b
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434722B2

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