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Sulfuryl chloride → [(Chlorocarbonyl)oxy]methyl 2-methylpropanoate

HRID 843092
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HRID 843092 반응식
C(S[C:4]([O:6][CH2:7][O:8][C:9](=[O:13])[CH:10]([CH3:12])[CH3:11])=[O:5])C.S(Cl)([Cl:17])(=O)=O>>[Cl:17][C:4]([O:6][CH2:7][O:8][C:9](=[O:13])[CH:10]([CH3:12])[CH3:11])=[O:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24648Sulfuryl chlorideHCID 85885666Isobutyric acid ethylsulfanylcarbonyloxymethyl ester

생성물 1

HCID 19067202[(Chlorocarbonyl)oxy]methyl 2-methylpropanoate

반응 조건

온도
-40 °C

실험 절차

A 100 mL roundbottom flask was charged with the 2-methylpropanoic acid ethylsulfanylcarbonyloxymethyl ester (2.91 g, 14.1 mmol) and cooled to −40° C. in an acetone dry ice bath. Sulfuryl chloride (1.90 g, 14.1 mmol) was added over one minute. After 10 minutes the acetone/dry ice cooling bath was removed and replaced with an ice/water bath. After 30 minutes of stirring, the cooling bath was removed and the reaction was allowed to stir for one hour at room temperature and then placed under vacuum for 90 minutes. The material was used without purification. 1H-NMR (300 MHz, CDCl3) δ (ppm): 1.22 (d, 6H), 2.65 (m, 1H), 5.83 (s, 2H).

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  1. customAfter 10 minutes the acetone/dry ice cooling bath was removed
  2. customreplaced with an ice/water bath
  3. customthe cooling bath was removed
  4. stirringto stir for one hour at room temperature
  5. waitplaced under vacuum for 90 minutes
  6. customThe material was used without purification

출처 및 근거

ORD 기록
ord-b73f26dc820f47d092217a32031e4425
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06376548B1

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