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Hydrochloric Acid → HCID 18963024、化合物

HRID 218245
ノート
印刷プレビュー

反応式

HRID 218245 の反応式
[Cl-].[Mg+2].[Cl-].[OH:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH2:11][CH3:12])[C:6]=1[OH:13].C(N(CC)CC)C.[CH2:21]=[O:22].Cl>C(#N)C.C(OCC)C>[OH:4][C:5]1[C:6]([OH:13])=[C:7]([CH2:11][CH3:12])[CH:8]=[CH:9][C:10]=1[CH:21]=[O:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 712FormaldehydeHCID 8471TriethylamineHCID 702783-Ethyl-1,2-benzenediolHCID 5360315Magnesium Chloride

生成物 1

HCID 18963024HCID 18963024、化合物収率 75.2%

試薬・触媒・溶媒 2

HCID 3283
Diethyl Ether
溶媒
HCID 6342Acetonitrile溶媒

実験手順

Magnesium chloride (1.71 g, 18 mmol) was added at room temperature to a solution of 10 (1 g, 7.2 mmol) in acetonitrile (10 mL), followed by triethylamine (6.3 mL, 45 mmol). Paraformaldehyde (1.47 g, 49 mmol) was then added portionwise to the stirred suspension and the mixture was heated at reflux for 2 hours. The mixture was cooled to room temperature then poured into a vigorously stirred mixture of 50 mL of 5% HCl and 50 mL of diethyl ether. The organic phase was separated, and the aqueous layer re-extracted with 50 mL of ether. The combined organic extracts were washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure to give a crude which was purified by column (cyclohexane:AcOEt 6:1) to give 0.9 g of 11:

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 2 hours
  3. customThe organic phase was separated
  4. extractionthe aqueous layer re-extracted with 50 mL of ether
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried over sodium sulphate
  7. customthe solvent removed under reduced pressure
  8. customto give a crude which
  9. customwas purified by column (cyclohexane:AcOEt 6:1)

出典と根拠

ORDレコード
ord-5146c969ce2a40989e4964e0b17f31bb
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08198302B2

反応ノート

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