تفاعل #414184

ord-0d01e251672f4789a72338a3ae6116cf

معادلة التفاعل

O=S(=O)(Cl)Cl
sulfonyl chloride
Cc1cccc(Cl)c1S(=O)(=O)Cl
2-chloro-6-methylbenzenesulfonyl chloride
CCOP(=O)(CO)OCC
diethyl P-(hydroxymethyl)phosphonate
CCN(CC)CC
triethylamine
CCOP(=O)(COS(=O)(=O)c1c(C)cccc1Cl)OCC
oil
المردود 87.2%
CCOP(=O)(COS(=O)(=O)c1c(C)cccc1Cl)OCC
Diethyl P-[[(2-chloro-6-methylphenyl)sulfonyloxy]methyl]phosphonate
المردود 87.2%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThe addition
  2. 2
    أخرىto form shortly
  3. 3
    workup.STIRRINGAfter 48 hours of additional stirring the reaction solution
  4. 4
    غسيلThe organic phase was washed with two 90 ml portions of water
  5. 5
    تجفيفdried with magnesium sulfate
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated

الإجراء التجريبي

A solution of 4.63 g of 2-chloro-6-methylbenzenesulfonyl chloride dissolved in 20 ml of anhydrous ether was added dropwise over a 15 minute period to a mixture of 3.50 g of diethyl P-(hydroxymethyl)phosphonate (Example 17), 5 ml of triethylamine and 15 ml of anhydrous ether. The addition was mildly exothermic and a white precipitate began to form shortly after the addition of the sulfonyl chloride was begun. The reaction was stirred at room temperature overnight. After 48 hours of additional stirring the reaction solution was diluted with 200 ml of ethyl acetate and 80 ml of water. The organic phase was washed with two 90 ml portions of water, dried with magnesium sulfate, filtered and concentrated to yield 6.4 g of an oil which solidified upon standing, mp 41°-43° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05272128uspto-grants-1993_12