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Methyl bromoacetate → 2-Methoxy-2-oxoethyl lactate

HRID 1491551
Notes
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Reaction equation

HRID 1491551 reaction equation
Br[CH2:2][C:3]([O:5][CH3:6])=[O:4].O.O.[C:9]([O-:14])(=[O:13])[CH:10]([CH3:12])[OH:11].C[N+](C)(C)C>CN(C)C=O>[C:9]([O:14][CH2:2][C:3]([O:5][CH3:6])=[O:4])(=[O:13])[CH:10]([CH3:12])[OH:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 60984Methyl bromoacetateHCID 18953226Tetramethylammonium lactate dihydrate

Product 1

HCID 197888162-Methoxy-2-oxoethyl lactate

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Methyl bromoacetate (4.73 mL, 50 mmol) was added to a stirring solution of tetramethylammonium lactate dihydrate (11.0 g, 55 mmol) in 20 mL dimethylformamide at room temperature. Tetramethylammonium bromide separated from the reaction mixture as a white solid and the title compound was formed quantitatively within 60 min as determined by CG (Method A). The reaction mixture was filtered, the solids were washed with ethyl ether, and the combinated filtrate and ether solution was washed with 5% NaCl/5% NaHCO3. Sufficient ethyl ether was added to effect rapid separation of the phases, the aqueous phase was extracted with CH2Cl2, and the organic phases were combined and dried with MgSO4. The solvent was removed and the resulting residue was distilled under reduced pressure to give the title compound: b.p. 79° C./0.15 mm Hg.

Workup

  1. customTetramethylammonium bromide separated from the reaction mixture as a white solid

Sources & evidence

ORD record
ord-05353004209740dea657c6e194a0e935
Source dataset
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05371001

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes