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Lithium Hydroxide → Lithium 2-methyl-2-(5-pyrimidinyl)propionate

HRID 2294941
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인쇄 미리보기

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HRID 2294941 반응식
[CH3:1][C:2]([C:9]1[CH:10]=[N:11][CH:12]=[N:13][CH:14]=1)([CH3:8])[C:3]([O:5]CC)=[O:4].[OH-].[Li+:16].C1COCC1>C(O)(=O)C>[CH3:8][C:2]([C:9]1[CH:14]=[N:13][CH:12]=[N:11][CH:10]=1)([CH3:1])[C:3]([O-:5])=[O:4].[Li+:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3939Lithium HydroxideHCID 8028TetrahydrofuranHCID 21471571Ethyl 2-methyl-2-(5-pyrimidinyl)propionate

생성물 1

HCID 23708609Lithium 2-methyl-2-(5-pyrimidinyl)propionate

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of ethyl 2-methyl-2-(5-pyrimidinyl)propionate (4.64 g), 1.0N lithium hydroxide (26 mL) and THF (100 mL) was heated to reflux under argon for 26 h. The mixture was allowed to cool, adjusted to pH 7 with acetic acid, and concentrated to dryness to give 4.11 g of lithium 2-methyl-2-(5-pyrimidinyl)propionate as a pale solid.

후처리

  1. temperaturewas heated
  2. temperatureto reflux under argon for 26 h
  3. temperatureto cool
  4. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-f05915991b0345408594eb1106f8a1bf
출처 데이터셋
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05691323

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