2-Methoxyethanol → HCID 14795651, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH2:4][OH:5].[Cl:6][CH:7]([O:9][C:10](Cl)=[O:11])[CH3:8]>C(Cl)Cl>[CH3:1][O:2][CH2:3][CH2:4][O:5][C:10](=[O:11])[O:9][CH:7]([Cl:6])[CH3:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 11.9 ml 2-Methoxy-ethanol and 17.98 ml 1-chloroethyl-chloroformate in 200 ml absolute CH2Cl2 13.3 ml pyridine were added at 5–10 ° C. in an argon atmosphere. The mixture was stirred at RT for 5 h and washed successively with 1 N HCl, with an aqueous solution of KHSO4/K2SO4 and water. The organic phase was dried over Na2SO4. After filtration, the solvent was removed in vacuo and the residue purified by destillation. Kp.=88° C. (5.5 mbar). Yield: 22.4 g.
Workup
- washwashed successively with 1 N HCl, with an aqueous solution of KHSO4/K2SO4 and water
- dry with materialThe organic phase was dried over Na2SO4
- filtrationAfter filtration
- customthe solvent was removed in vacuo
- customthe residue purified by destillation
- custom=88° C. (5.5 mbar)
Sources & evidence
- ORD record
- ord-4a3b61047d5a4859a362b4fcad0bc345
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196103B2
Reaction notes
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