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Thionyl Chloride → HCID 10355913, 화합물

HRID 1246326
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HRID 1246326 반응식
[CH2:1]([O:5][C:6]1[C:14]([O:15][CH3:16])=[CH:13][C:9]([C:10](O)=[O:11])=[CH:8][C:7]=1[O:17][CH3:18])[CH2:2][CH2:3][CH3:4].S(Cl)([Cl:21])=O>C1(C)C=CC=CC=1>[CH2:1]([O:5][C:6]1[C:14]([O:15][CH3:16])=[CH:13][C:9]([C:10]([Cl:21])=[O:11])=[CH:8][C:7]=1[O:17][CH3:18])[CH2:2][CH2:3][CH3:4]
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참가 물질

4

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HCID 24386Thionyl ChlorideHCID 104450144-Butoxy-3,5-dimethoxybenzoic acid

생성물 1

HCID 10355913HCID 10355913, 화합물수율 99%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
90 °C

실험 절차

A mixture of 4-butyloxy-3,5-dimethoxybenzoic acid (5.0 g, 0.0197 mol) and thionyl chloride (10 mL) in toluene (10 mL) was heated at 90° C. for 18 h. The reaction mixture was concentrated under reduced pressure. To remove excess of thionyl chloride the residue was repeatedly redissolved in toluene (3×20 mL) and the resulting solution evaporated to dryness to obtain 4-butyloxy-3,5-dimethoxybenzoyl chloride (5.3 g, 99% yield) as a pale yellow oil. 1H NMR (CDCl3) δ: 0.99 (t, J=5.0 Hz, 3H), 1.47 (m, 2H), 1.73 (m, 2H), 3.90 (s, 6H), 4.09 (t, J=5.1 Hz, 2H), 7.36 (s, 2H).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customTo remove excess of thionyl chloride the residue
  3. dissolutionwas repeatedly redissolved in toluene (3×20 mL)
  4. customthe resulting solution evaporated to dryness

출처 및 근거

ORD 기록
ord-725d6d35313e44d6b0d697ffd54a8665
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07126027B2

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