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3-Acetyl-alpha,alpha-dimethylbenzyl isocyanate → 3-Acetyl-alpha,alpha-dimethylbenzylamine

HRID 64231
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HRID 64231 반응식
[C:1]([C:4]1[CH:5]=[C:6]([CH:13]=[CH:14][CH:15]=1)[C:7]([N:10]=C=O)([CH3:9])[CH3:8])(=[O:3])[CH3:2]>Cl>[C:1]([C:4]1[CH:5]=[C:6]([CH:13]=[CH:14][CH:15]=1)[C:7]([NH2:10])([CH3:9])[CH3:8])(=[O:3])[CH3:2]
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참가 물질

3

반응물 1

HCID 715003593-Acetyl-alpha,alpha-dimethylbenzyl isocyanate

생성물 1

HCID 698237233-Acetyl-alpha,alpha-dimethylbenzylamine수율 55%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

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온도
0 °C

실험 절차

3-Acetyl-α, α-dimethylbenzyl isocyanate 3 (1000 mg, 4.92 mmol) in 8N HCl (30 mL) were refluxed for 30 min. The reaction mixture was cooled to 0° C. and then washed with diethyl ether. The aqueous portion was neutralized with a 10% NaOH solution and extracted with diethyl ether (3×20 mL). The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered and concentrated. The residue was purified by chromatography eluting with methanol/chloroform to give 24 as a yellow oil (478 mg, 55%). 1H NMR (CDCl3, 400 MHz) δ 1.57 (s, 6H), 2.61 (s, 3H), 3.72 (s, 2H), 7.43 (t, J=7.6 Hz, 1H), 7.75 (d, J=7.6 Hz, 1H), 7.82 (d, J=7.6 Hz, 1H), 8.14 (s, 1H).

후처리

  1. washwashed with diethyl ether
  2. extractionextracted with diethyl ether (3×20 mL)
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over anhydrous MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by chromatography
  8. washeluting with methanol/chloroform

출처 및 근거

ORD 기록
ord-e4b682ed87154c24a98b02009df115c8
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447134B2

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