Ethyl (diethoxyphosphoryl)methanesulfonate → HCID 86632005, compound

HRID 2283276Notes

Reaction equation

HRID 2283276 reaction equation
C([Li])CCC.[CH2:6]([O:8][S:9]([CH2:12]P(OCC)(OCC)=O)(=[O:11])=[O:10])[CH3:7].[Cl:21][C:22]1[CH:29]=[CH:28][C:25]([CH:26]=O)=[C:24]([O:30][CH3:31])[CH:23]=1>C1COCC1>[CH2:6]([O:8][S:9]([CH:12]=[CH:26][C:25]1[CH:28]=[CH:29][C:22]([Cl:21])=[CH:23][C:24]=1[O:30][CH3:31])(=[O:10])=[O:11])[CH3:7]

Participants

5

Conditions

Temperature
-78 °C

Procedure

A 2.5M solution of n-butyllithium in hexanes (6.15 mL, 15.37 mmol) was added dropwise to a stirred solution of (diethoxy-phosphoryl)-methanesulfonic acid ethyl ester (4.0 g, 15.37 mmol) in THF (200 mL) at −78° C. The reaction mixture was stirred at −78° C. for 15 minutes. A solution of 4-chloro-2-methoxy-benzaldehyde (2.41 g, 14.10 mmol) in THF (20 mL) was then added dropwise. After the addition was complete the reaction mixture was warmed to RT, stirred for 1 h and quenched with brine. The reaction mixture was concentrated under reduced pressure and DCM (200 mL) was added. The organic layer was separated, washed with brine (3×100 mL) and dried over MgSO4. Removal of solvent under reduced pressure, followed by purification on silica gel using hexane/ethyl acetate, 4:1 to 2:1 afforded the title compound (3.90 g, quantitative) as a white solid.

Workup

  1. additionAfter the addition
  2. temperaturewas warmed to RT
  3. stirringstirred for 1 h
  4. customquenched with brine
  5. concentrationThe reaction mixture was concentrated under reduced pressure and DCM (200 mL)
  6. additionwas added
  7. customThe organic layer was separated
  8. washwashed with brine (3×100 mL)
  9. dry with materialdried over MgSO4
  10. customRemoval of solvent under reduced pressure
  11. customfollowed by purification on silica gel

Sources & evidence

ORD record
ord-d198b11761a14ecd9dc4185597adb463
Source dataset
uspto-grants-2015_09
Patent number
US09145380B2

Reaction notes

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