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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl bromoacetate → 2-Methoxy-2-oxoethyl lactate

HRID 1491551
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HRID 1491551 반응식
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]
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참가 물질

4

반응물 2

HCID 60984Methyl bromoacetateHCID 18953226Tetramethylammonium lactate dihydrate

생성물 1

HCID 197888162-Methoxy-2-oxoethyl lactate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-05353004209740dea657c6e194a0e935
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05371001

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