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Methanesulfonic Acid → 5-Dimethylaminomethylfurfuryl chloride hydrochloride

HRID 1379895
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HRID 1379895 반응식
[ClH:1].[CH3:2][N:3]([CH2:5][C:6]1[O:12][C:9]([CH2:10]O)=[CH:8][CH:7]=1)[CH3:4].S(Cl)([Cl:15])=O.CS(O)(=O)=O>C(#N)C>[ClH:15].[CH3:2][N:3]([CH2:5][C:6]1[O:12][C:9]([CH2:10][Cl:1])=[CH:8][CH:7]=1)[CH3:4]
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참가 물질

5

반응물 3

HCID 6395Methanesulfonic AcidHCID 24386Thionyl Chloride2회HCID 3086123((2-(Hydroxymethyl)-5-furyl)methyl)ammonium chloride

생성물 1

HCID 129547925-Dimethylaminomethylfurfuryl chloride hydrochloride

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
10 °C

실험 절차

Combine 5-[(dimethylamino)methyl]-furfuryl alcohol hydrochloride (1.72 kg, 8.97 mol) and acetonitrile (4.3 L). Cool to about 10° C. Add thionyl chloride (1.02 kg, 8.54 mol) dropwise, while maintaining the temperature of the reaction at below about 40° C. After the addition of thionyl chloride is complete, add methanesulfonic acid (1.3 kg, 13.5 mol). Distill to remove about 1.8 L of distillate to give the title compound as a solution.

후처리

  1. customthe temperature of the reaction at below about 40° C
  2. distillationDistill
  3. customto remove about 1.8 L of distillate

출처 및 근거

ORD 기록
ord-82f011ea3df240f298bd03a1f2836efc
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05672724

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