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Sodium Hydroxide → 2-Carboxy-3-chloro-4-(hydroxymethyl)thiophene

HRID 370087
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HRID 370087 반응식
C[O:2][C:3]([C:5]1[S:6][CH:7]=[C:8]([CH2:11][O:12]C(=O)C)[C:9]=1[Cl:10])=[O:4].[OH-].[Na+]>O1CCOCC1.O>[C:3]([C:5]1[S:6][CH:7]=[C:8]([CH2:11][OH:12])[C:9]=1[Cl:10])([OH:4])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 183769232-Methoxycarbonyl-3-chloro4-(acetoxymethyl)thiophene

생성물 1

HCID 183769972-Carboxy-3-chloro-4-(hydroxymethyl)thiophene수율 99.1%

시약·촉매·용매 2

HCID 962Water용매HCID 312751,4-Dioxane용매

실험 절차

To a solution of 2-methoxycarbonyl-3-chloro-4-(acetoxymethyl)thiophene (83 g, 0.33 mol) in 1,4-dioxane (350 mL) was added a solution of sodium hydroxide (26.5 g, 0.66 mol) in water (200 mL) and the mixture stirred at ambient temperature. After 1 hour the dioxane was removed in vacuo and the aqueous solution washed with ethyl acetate (2×1 00 mL). The aqueous layer was brought to pH 2 by addition of concentrated HCl, then extracted with n-butanol (4×200 mL). The combined extracts were concentrated and the resulting solid dried in vacuo to afford 63 g (90% yield) of 2-carboxy-3-chloro-4-(hydroxymethyl)thiophene as a tan powder; NMR (DMSO-d6) 7.7 (s, 1), 4.4 (s, 2) ppm.

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후처리

  1. customAfter 1 hour the dioxane was removed in vacuo
  2. washthe aqueous solution washed with ethyl acetate (2×1 00 mL)
  3. additionThe aqueous layer was brought to pH 2 by addition of concentrated HCl
  4. extractionextracted with n-butanol (4×200 mL)
  5. concentrationThe combined extracts were concentrated
  6. customthe resulting solid dried in vacuo

출처 및 근거

ORD 기록
ord-0c7168b80f8f469c8c947228f5310878
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06140351

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