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Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate

HRID 333077
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HRID 333077 반응식
[CH3:1][S:2]([O:5][CH2:6][CH3:7])(=[O:4])=[O:3].[Li+].CCC[CH2-].[P:13](Cl)(=[O:20])([O:17][CH2:18][CH3:19])[O:14][CH2:15][CH3:16]>O1CCCC1>[CH2:15]([O:14][P:13]([CH2:1][S:2]([O:5][CH2:6][CH3:7])(=[O:4])=[O:3])([O:17][CH2:18][CH3:19])=[O:20])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6113Ethyl MethanesulfonateHCID 13139Diethyl chlorophosphateHCID 61028n-Butyl lithium

생성물 1

HCID 10934205Ethyl (diethoxyphosphoryl)methanesulfonate수율 117.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of ethyl methanesulfonate (4.14 mL, 40.2 mmol) in anhydrous tetrahydrofuran (100 ml) was cooled to −78° C. under a nitrogen atmosphere. N-Butyllithium (20 ml, 50.0 mmol) was added slowly in 7 minutes after which stirring was continued for 15 minutes. Diethyl phosphorochloridate (4.36 mL, 30.2 mmol) was added, the reaction mixture was stirred for 2.5 h, the cooling bath was removed and the mixture was allowed to reach room temperature. The reaction mixture was quenched with aqueous saturated ammonium chloride (150 ml) and the resulting mixture was extracted with EtOAc (2×100 ml). The combined extracts were dried over sodium sulfate and concentrated under reduced pressure to yield 9.20 g of a yellow oil. The oil was purified over silicagel (600 g) using a gradient of ethyl acetate (0-100%) in heptane to yield 1.75 g of the product (6.7 mol, 17%).

후처리

  1. stirringthe reaction mixture was stirred for 2.5 h
  2. customthe cooling bath was removed
  3. customto reach room temperature
  4. customThe reaction mixture was quenched with aqueous saturated ammonium chloride (150 ml)
  5. extractionthe resulting mixture was extracted with EtOAc (2×100 ml)
  6. dry with materialThe combined extracts were dried over sodium sulfate
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-40d13101437a4e78a60ba9d76cfe0aff
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877934B2

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