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HRID 22055作成日:2026年10月23日

3-Nitrobenzoic acid → Biphenyl indolizinyl nitrobenzoate

https://huagongshe.com/ja/reaction/22055

反応式

関与物質

役割名称HCID仕込み量
反応物3-Nitrobenzoic acidHCID 8497—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物HCID 178516797HCID 178516797—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Biphenyl indolizinyl nitrobenzoateHCID 86748744—

反応手順

Alternatively, the biphenyl trans-hydroxy triazole can be prepared using the Mitsunobu reaction conditions. To a solution of diethyl azodicarboxylate (2.0 mmol) and 3-nitrobenzoic acid (2.0 mmol) in 2.0 mL of THF is added dropwise a solution of the biphenyl hydroxy triazole (2.0 mmol, obtained from Step 1 of Example 3224), and triphenylphosphine (2.0 mmol) in 1.0 mL of THF at room temperature. The resulting solution is stirred at room temperature until the reaction is complete. The resulting mixture is diluted with ether or ethyl acetate, and washed with water. The extracts are dried (MgSO4) and concentrated in vacuo to give the biphenyl indolizinyl nitrobenzoate. The crude benzoate is hydrolyzed with LiOH in aqueous THF at room temperature and purified to give the biphenyl trans-hydroxy triazole.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426105
出典データセットuspto-grants-1995_06
ORD IDord-23ceeef732bc4310a67a7ccc06fd3328
出典メモuspto-grants-1995_06