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HCID 332828, 화합물 → 4-(1,3-Dioxaindan-5-yl)oxane-2,6-dione

HRID 1243517
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HRID 1243517 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]([CH2:15][C:16]([OH:18])=[O:17])[CH2:11][C:12]([OH:14])=O)=[CH:9][C:4]=2[O:3][CH2:2]1>C(OC(=O)C)(=O)C>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]3[CH2:11][C:12](=[O:14])[O:18][C:16](=[O:17])[CH2:15]3)=[CH:9][C:4]=2[O:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 332828HCID 332828, 화합물

생성물 1

HCID 219278554-(1,3-Dioxaindan-5-yl)oxane-2,6-dione수율 70.3%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

3-(1,3-benzodioxol-5-yl)pentanedioic acid (2 g, 7.9 mmoles) was suspended in acetic anhydride (50 ml) and refluxed for two hours. The reaction mixture was allowed to cool to room temperature and the solvent was removed under reduced pressure. The residue was triturated with ether to give the product (1.3 g, 70%). 1H NMR (DMSO-d6) δ 6.91 (m, 1H), 6.89 (m, 1H), 6.72 (m, 1H), 6.01 (s, 2H), 3.53–3.41 (m, 1H), 3.07–2.89 (m, 4H).

후처리

  1. temperaturerefluxed for two hours
  2. customthe solvent was removed under reduced pressure
  3. customThe residue was triturated with ether

출처 및 근거

ORD 기록
ord-b78362e570a04da3afa2180bb2364655
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07119098B2

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