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Hydrochloric Acid → 6-(Hydroxymethyl)-2-benzofuran-1(3H)-one

HRID 2080899
ノート
印刷プレビュー

反応式

HRID 2080899 の反応式
C[O:2][C:3](=[O:14])[C:4]1[CH:9]=[C:8]([CH2:10]Br)[CH:7]=[CH:6][C:5]=1[CH2:12]Br.C(=O)([O-])[O-:16].[Ca+2].Cl>O1CCOCC1>[OH:16][CH2:10][C:8]1[CH:9]=[C:4]2[C:5]([CH2:12][O:2][C:3]2=[O:14])=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 10112Calcium CarbonateHCID 12633556Methyl 2,5-bis(bromomethyl)benzoate

生成物 1

HCID 178625846-(Hydroxymethyl)-2-benzofuran-1(3H)-one

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

The compound (1.1274 g) obtained in Example 102-1 was dissolved in carbon tetrachloride (19.2 ml). The reaction solution was added with N-bromosuccinimide (2.417 g) and benzoyl peroxide (147.2 mg), and the whole was refluxed under heating for 6.5 hours. After having been cooled to room temperature, the reaction solution was concentrated under reduced pressure. The resultant residue was purified through silica gel column chromatography (hexane/ethyl acetate), thereby obtaining a mixture (2.4003 g) containing 2,5-bis-bromomethyl-benzoic acid methyl ester. The resultant mixture was dissolved in a 50% 1,4-dioxane aqueous solution (48 ml). The reaction solution was added with calcium carbonate (3.4823 g) and the whole was stirred at 100° C. for 16.5 hours. After having been cooled to room temperature, the reaction solution was cooled to 0° C. and concentrated hydrochloric acid was gradually added thereto to make the pH of the solution to 2. After that, the whole was stirred at room temperature for 20 minutes. The reaction solution was subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and a saturated saline solution and then dried with anhydrous sodium sulfate. After the drying agent was filtrated out, the filtrate was concentrated under reduced pressure. The resultant residue was purified through silica gel column chromatography (chloroform/ethyl acetate), thereby obtaining the subject compound (372.0 mg) as a white crystal.

後処理

  1. temperatureAfter having been cooled to room temperature
  2. temperaturethe reaction solution was cooled to 0° C.
  3. stirringAfter that, the whole was stirred at room temperature for 20 minutes
  4. extractionThe reaction solution was subjected to extraction with ethyl acetate
  5. washThe organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution
  6. dry with materiala saturated saline solution and then dried with anhydrous sodium sulfate
  7. filtrationAfter the drying agent was filtrated out
  8. concentrationthe filtrate was concentrated under reduced pressure
  9. customThe resultant residue was purified through silica gel column chromatography (chloroform/ethyl acetate)

出典と根拠

ORDレコード
ord-dd8b359fd6704c9a804b253937db5d7d
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07932281B2

反応ノート

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