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Triethylamine → 4-Isocyanato-4-methyloxane

HRID 1798924
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HRID 1798924 반응식
C[C:2]1([C:8](O)=O)[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.C([N:13]([CH2:16]C)CC)C.P(N=[N+]=[N-])(OC1C=CC=CC=1)(OC1C=CC=CC=1)=[O:19].[OH-].[Na+]>C1(C)C=CC=CC=1>[N:13]([C:2]1([CH3:8])[CH2:3][CH2:4][O:5][CH2:6][CH2:7]1)=[C:16]=[O:19]
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 123414Diphenylphosphoryl azideHCID 115718204-METHYLTETRAHYDRO-2H-PYRAN-4-CARBOXYLIC ACID

생성물 1

HCID 722137684-Isocyanato-4-methyloxane수율 42.1%

시약·촉매·용매 1

HCID 1140Toluene용매
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

반응 조건

온도
85 °C

실험 절차

A stirred solution of 4-methyltetrahydro-2H-pyran-4-carboxylic acid (D9) (1.26 g, 8.74 mmol) in Toluene (50 mL) at room temperature under argon was treated with triethylamine (1.58 mL, 11.36 mmol) and diphenyl azidophosphate (1.88 mL, 8.74 mmol) and heated to 85° C. for 2 hr. The mixture was allowed to cool to room temperature, then treated with 1 M NaOH solution (40 mL) and extracted with Et2O (3×). The combined extract was dried (Na2SO4), filtered and concentrated under vacuum to give the title compound (D10) (520 mg, 34%) as a yellow oil.

후처리

  1. temperatureto cool to room temperature
  2. extractionextracted with Et2O (3×)
  3. extractionThe combined extract
  4. dry with materialwas dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-8e1e05a3adb44435b5551640396cee20
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08344000B2

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