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2,6-Lutidine → (5-Oxotetrahydrofuran-3-yl)methyl trifluoromethanesulfonate

HRID 2201242
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HRID 2201242 반응식
[F:1][C:2]([F:15])([F:14])[S:3]([O:6]S(C(F)(F)F)(=O)=O)(=[O:5])=[O:4].O[CH2:17][CH:18]1[CH2:22][O:21][C:20](=[O:23])[CH2:19]1.N1C(C)=CC=CC=1C>C(Cl)Cl>[F:1][C:2]([F:15])([F:14])[S:3]([O:6][CH2:17][CH:18]1[CH2:19][C:20](=[O:23])[O:21][CH2:22]1)(=[O:5])=[O:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 79372,6-LutidineHCID 67749Trifluoromethanesulfonic anhydrideHCID 99640814-(Hydroxymethyl)oxolan-2-one

생성물 1

HCID 86723477(5-Oxotetrahydrofuran-3-yl)methyl trifluoromethanesulfonate

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

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온도
0 °C
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실험 절차

A solution of trifluoromethanesulfonic anhydride (15.0 g, 53.2 mmol) in DCM (25 mL) was added dropwise to a solution of 4-(hydroxymethyl)dihydrofuran-2(3H)-one (4.75 g, 41.0 mmol) and 2,6-lutidine (7.15 mL, 61.4 mmol) in DCM (111 mL) at 0° C. The mixture was stirred at 0° C. for 20 minutes. The product mixture was diluted with DCM (100 mL) and was washed with water (3×100 mL). The organic phase was dried over magnesium sulfate and evaporated under vacuum.

후처리

  1. washwas washed with water (3×100 mL)
  2. dry with materialThe organic phase was dried over magnesium sulfate
  3. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-d0a057e4dd90443ebb449ded3dd0e580
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09359381B2

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