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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Methyl-5-(2-hydroxyethyl)thiazole → 103871-46-1

HRID 2396403
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인쇄 미리보기

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HRID 2396403 반응식
[OH:1][CH2:2][CH2:3][C:4]1[S:8][CH:7]=[N:6][C:5]=1[CH3:9].[Br:10][CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13]>C(O)C>[Br-:10].[CH2:15]([O:14][C:12]([CH2:11][N+:6]1[C:5]([CH3:9])=[C:4]([CH2:3][CH2:2][OH:1])[S:8][CH:7]=1)=[O:13])[CH3:16]
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참가 물질

4

반응물 2

HCID 11364-Methyl-5-(2-hydroxyethyl)thiazoleHCID 7748Ethyl bromoacetate

생성물 1

HCID 10935796103871-46-1수율 71.7%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
0 °C

실험 절차

A solution of 5-(2-hydroxyethyl)-4-methylthiazole (306 g) and ethyl bromoacetate (356.2 g) in ethanol (1 L) was heated to reflux. After two hours, the ethanol was removed by distillation and the residue treated with isopropanol (1.5 L). The resulting solution was cooled to about 0° C., causing crystallization of compound 1. After three hours, the crystalline material was separated from the mother liquor. Additional crystals were obtained by prolonged cooling of the mother liquor at 0° C. Combination of the crystalline material gave 474.3 g of compound 1. Melting point 96°-98° C.

후처리

  1. customthe ethanol was removed by distillation
  2. additionthe residue treated with isopropanol (1.5 L)
  3. customcrystallization of compound 1
  4. waitAfter three hours
  5. customthe crystalline material was separated from the mother liquor
  6. customAdditional crystals were obtained
  7. temperatureby prolonged cooling of the mother liquor at 0° C

출처 및 근거

ORD 기록
ord-2199beb11d7f418cb85e9ee5a0f469e2
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05491241

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