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Methyl bromoacetate → 2-Methoxy-2-oxoethyl lactate

HRID 1491551
ノート
印刷プレビュー

反応式

HRID 1491551 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 60984Methyl bromoacetateHCID 18953226Tetramethylammonium lactate dihydrate

生成物 1

HCID 197888162-Methoxy-2-oxoethyl lactate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-05353004209740dea657c6e194a0e935
出典データセット
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05371001

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート