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Diethyl Ether → 4-isobutyloxybenzyl isocyanate

HRID 852282
ノート
印刷プレビュー

反応式

HRID 852282 の反応式
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12]C(O)=O)=[CH:8][CH:7]=1)[CH:2]([CH3:4])[CH3:3].CN(C1C2C([N:29]([CH3:31])C)=CC=CC=2C=CC=1)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:39])C=CC=CC=1.C(OCC)C>C1COCC1>[CH2:1]([O:5][C:6]1[CH:7]=[CH:8][C:9]([CH2:12][N:29]=[C:31]=[O:39])=[CH:10][CH:11]=1)[CH:2]([CH3:3])[CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 3283Diethyl EtherHCID 88675Proton spongeHCID 199401P,P-Diphenylphosphinic azideHCID 12199197[4-(2-Methylpropoxy)phenyl]acetic acid

生成物 1

HCID 574300934-isobutyloxybenzyl isocyanate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

4-isobutoxyphenylacetic acid (7.6 g, 36.5 mmol) was dissolved in THF (50 mL). Proton Sponge™ (8.2 g, 38 mmol) was added, and the mixture was stirred for 15 min. Diphenylphosphoryl azide (10.6 g, 38 mmol) was added dropwise and the mixture was heated to reflux for 4 h. The mixture was cooled to room temperature and placed in the freezer at −18° C. for 20 h. The resulting white precipitate was vigorously stirred with diethyl ether (250 mL) for 15 min and filtered. The filtrate was evaporated to give crude 4-isobutoxybenzyl isocyanate (1.97 g, 9.6 mmol), which was dissolved in dichloromethane (50 mL) and added to a solution of 50ELH85 (2.91 g, 9.6 mmol) in dichloromethane (50 mL). The reaction mixture was stirred for 20 h and concentrated. The crude product was purified by flash chromatography (0–5% methanol in dichloromethane) to give N-(4-fluorobenzyl)-N-[1-(trifluoroacetyl)piperidin-4-yl]-N′-(4-isobutyloxybenzyl)carbamide (76ELH17, 3.90 g, 91%).

後処理

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 4 h
  3. waitplaced in the freezer at −18° C. for 20 h
  4. filtrationfiltered
  5. customThe filtrate was evaporated

出典と根拠

ORDレコード
ord-2326d9a400604ee29071532ea2beb037
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07253186B2

反応ノート

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