Sodium Chloride → 1,4-Dioxa-8-azaspiro(4.5)decane

HRID 1508356ノート

反応式

HRID 1508356 の反応式
[OH-].[Na+].Cl.[O:4]1[C:8]2([CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[O:7][CH2:6][CH2:5]1.[Cl-].[Na+]>O>[O:4]1[C:8]2([CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[O:7][CH2:6][CH2:5]1

参加物

5

実験手順

To a 30 L reactor equipped with a mechanic stirrer, an addition funnel and a septum was charged sodium hydroxide (NaOH, 1.4 kg, 35 mol, 2.0 equiv) and water (7 L) and the resulting solution was treated with 1,4-dioxa-8-azaspiro[4.5]decane hydrochloride (3.13 kg, 17.43 mol) at ambient temperature. The resulting mixture was then stirred at ambient temperature for 30 minutes before being saturated with solid sodium chloride (1.3 kg) and extracted with 2-methyl-tetrahydrofuran (3×7 L). The combined organic phase was dried with anhydrous sodium sulfate (Na2SO4, 1.3 kg) and concentrated under reduced pressure (70 mmHg) at 50° C. after removal of the drying reagent, sodium sulfate (Na2SO4), by filtration. The yellow oil thus obtained was distilled under reduced pressure (80 mmHg, by 115 to 120° C.) to afford 1,4-dioxa-8-azaspiro[4.5]decane (2.34 kg, 2.496 kg theoretical, 93.8%) as a clear oil, which was used directly in the subsequent coupling reaction.

後処理

  1. customTo a 30 L reactor equipped with a mechanic stirrer, an addition funnel
  2. extractionextracted with 2-methyl-tetrahydrofuran (3×7 L)
  3. dry with materialThe combined organic phase was dried with anhydrous sodium sulfate (Na2SO4, 1.3 kg)
  4. concentrationconcentrated under reduced pressure (70 mmHg) at 50° C.
  5. customafter removal of the drying reagent, sodium sulfate (Na2SO4)
  6. filtrationby filtration
  7. customThe yellow oil thus obtained
  8. distillationwas distilled under reduced pressure (80 mmHg, by 115 to 120° C.)

出典と根拠

ORDレコード
ord-0d124a7bb7c94b7ca2d0ff33af45ef20
出典データセット
uspto-grants-2015_12
特許番号
US09221845B2

反応ノート

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