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HRID 509302作成日:2026年10月24日

Triphenylphosphine → Methyl 4-{[[(2,4-dinitrophenyl)sulfonyl]({1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}methyl)amino]methyl}benzoate

https://huagongshe.com/ja/reaction/509302

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物(1-((Trimethylsilyl)methyl)-1h-1,2,3-triazol-4-yl)methanolHCID 59627317—
反応物Methyl 4-({[(2,4-dinitrophenyl)sulfonyl]amino}methyl)benzoateHCID 59627340—
溶媒BenzeneHCID 241—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 4-{[[(2,4-dinitrophenyl)sulfonyl]({1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}methyl)amino]methyl}benzoateHCID 59627272—

反応手順

A solution of {1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}methanol (241 mg, 1.30 mmol), methyl 4-({[(2,4-dinitrophenyl)sulfonyl]amino}methyl)benzoate (514 mg, 1.30 mmol), triphenylphosphine (409 mg, 1.56 mmol) and benzene (4.34 mL) was treated with diethylazodicarboxylate (247 uL, 1.56 mmol). After one hour additional portions of triphenylphosphine (204 mg, 0.780 mmol) and diethylazodicarboxylate (124 uL, 0.780 mmol) The reaction was diluted with EtOAc and washed with 2M aq. HCl 2×, water, brine, dried (MgSO4) and concentrated to afford a brown oil used crude in the next reaction. MS: cal'd 563 (MH+), exp 563 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096559B2
出典データセットuspto-grants-2015_08
ORD IDord-fbd65a37cabb4723994529d43b4a7427
出典メモuspto-grants-2015_08