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Iodoethane → Methyl 3-ethoxy-4-methoxybenzoate

HRID 612051
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인쇄 미리보기

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HRID 612051 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6].C(=O)([O-])[O-].[K+].[K+].[CH2:20](I)[CH3:21]>CN(C)C=O>[CH2:20]([O:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6])[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6340Iodoethane2회HCID 11430Potassium Carbonate2회HCID 4056967Methyl 3-hydroxy-4-methoxybenzoate

생성물 1

HCID 10536413Methyl 3-ethoxy-4-methoxybenzoate수율 55.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

A mixture of 24.3 g (134 mmol) of methyl 3-hydroxy-4-methoxybenzoate, 36.8 g (267 mmol) of anhyd potassium carbonate and 31.4 g (201 mmol) of ethyl iodide in 500 mL of dimethylformamide was stirred at 100° C. for 5.5 h. An additional amount of ethyl iodide (31.4 g) and potassium carbonate (18.4 g) was added and heating was continued for 2 h more. The reaction was filtered and volatile material was removed from the filtrate in vacuo. The residue was slurried with water and filtered to collect the product which was washed with water and dried. Recrystallization from heptane gave 15.6 g of methyl 3-ethoxy-4-methoxybenzoate as white crystals: mass spectrum (electrospray, m/e): M+H 210.9.

후처리

  1. temperatureheating
  2. waitwas continued for 2 h
  3. filtrationThe reaction was filtered
  4. customvolatile material was removed from the filtrate in vacuo
  5. filtrationfiltered
  6. customto collect the product which
  7. washwas washed with water
  8. customdried
  9. customRecrystallization from heptane

출처 및 근거

ORD 기록
ord-c13c2ef738e34b6f9b1bd7364d376e0c
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06002008

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