电化学促使α-重氮酯的磷酸化构筑亚膦酸腙

doi:10.6023/cjoc202309022

有机化学 ›› 2024, Vol. 44 ›› Issue (3): 1013-1020.DOI: 10.6023/cjoc202309022 上一篇下一篇

研究论文

电化学促使α-重氮酯的磷酸化构筑亚膦酸腙

孙雪, 颜廷涛, 闫克鲁, 杨建静^*(), 文江伟^*()

曲阜师范大学化学与化工学院山东省高校绿色天然产物与医药中间体重点实验室山东曲阜 273165

收稿日期:2023-09-21 修回日期:2023-11-13 发布日期:2024-04-02
通讯作者: 杨建静, 文江伟
作者简介:
† 共同第一作者
基金资助:
国家自然科学基金(21902083); 山东省自然科学基金(ZR2020QB130); 曲阜师范大学人才启动基金(6132); 曲阜师范大学人才启动基金(6125)

Electrochemical Enabled Phosphorylation of α-Diazoester to Access Phosphinic Hydrazone

Xue Sun, Tingtao Yan, Kelu Yan, Jianjing Yang(), Jiangwei Wen()

Key Laboratory of Green Natural Products and Pharmaceutical Intermediates in Colleges and Universities of Shandong Province, School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165

Received:2023-09-21 Revised:2023-11-13 Published:2024-04-02
Contact: Jianjing Yang, Jiangwei Wen
About author:
† The authors contributed equally to this work.
Supported by:
National Natural Science Foundation of China(21902083); Natural Science Foundation of Shandong Province(ZR2020QB130); Talent Program Foundation of Qufu Normal University(6132); Talent Program Foundation of Qufu Normal University(6125)

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摘要/Abstract

亚膦酸腙是一种罕见的结构片段, 有望应用于医药、功能材料、配体和合成中间体. 报道了一种牺牲阳极镍电极形成Ni^2＋以促进α-重氮酯磷酸化构筑亚膦酸腙的电化学方法. 反应在恒电流下进行, 无需外加贵金属催化剂和化学氧化还原试剂, 具有良好的底物适用性. 机理研究证实了成对电解介导的催化机制占主导地位.

关键词: 电化学, 牺牲阳极, 磷酸化, α-重氮酯, 亚磷酸腙

The phosphonic hydrazone represents a rare molecular fragment with promising applications in the fields of pharmaceuticals, functional materials, ligands, and synthetic intermediates. A novel electrochemical approach is presented for the generation of Ni^2＋ ions from sacrificial anode nickel, facilitating the phosphorylation of α-diazoester to construct phosphite hydrazone. The reaction was performed in an undivided cell in absence of precious metal catalyst and chemical redox reagent, exhibiting good substrate applicability. The mechanistic investigation has confirmed the predominant role of paired electrolysis in mediating the catalytic mechanism.

Key words: electrochemistry, sacrificial anode, phosphorylation, α-diazoester, phosphinic hydrazine

引用此文

孙雪, 颜廷涛, 闫克鲁, 杨建静, 文江伟. 电化学促使α-重氮酯的磷酸化构筑亚膦酸腙[J]. 有机化学, 2024, 44(3): 1013-1020.

Xue Sun, Tingtao Yan, Kelu Yan, Jianjing Yang, Jiangwei Wen. Electrochemical Enabled Phosphorylation of α-Diazoester to Access Phosphinic Hydrazone[J]. Chinese Journal of Organic Chemistry, 2024, 44(3): 1013-1020.

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图/表 6

Scheme 1. Selective functionalization of α-diazoesters

Entry	Deviation from standard conditions	Yield^b/%
1	None	98
2	Without current	n.d.
3	ⁿBu₄NClO₄, ⁿBu₄NBr, ⁿBu₄NOAc, Et₄NBr, Et₄NTs instead of ⁿBu₄NBF₄	45~82
4	LiClO₄ instead of ⁿBu₄NBF₄	n.d.
5	CH₃CN as solvent	53
6	DCE as solvent	82
7	DMSO as solvent	77
8	Pt(＋)\|Ni(－)	n.d.
9	Pt(＋), or C rods (＋) instead of Ni(＋)	n.d.
10	C rods(－), or Ni(－) instead of Pt(－)	85, 90
11	3 mA, 5 h	88
12	8 mA, 2 h	85

Table 1. Optimization of reaction conditionsa

Table 2. Substrate scope of α-diazoester and diaryl phosphorus oxidesa

Scheme 2. Large-scale synthesis of 1c and transformation

Scheme 3. Study on mechanism of electrochemical phosphorylation of α-diazoester (a) Radical inhibition experiments. (b) Metal ion verification experiments. (c) Working electrode verification experiments. (d) CV experiments: Ni net (1.0 cm×1.0 cm) as the working electrode, Pt plate (1.0 cm×1.0 cm) as the counter electrode, Ag/AgCl as the reference electrode, nBu4BF4 (0.15 mmol), CH2Cl2 (10.0 mL), 1a (0.25 mmol/L), 1b (0.25 mmol/L)

Scheme 4. Possible mechanism of electrochemical enabled phosphorylation of α-diazoester

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电化学促使α-重氮酯的磷酸化构筑亚膦酸腙

Electrochemical Enabled Phosphorylation of α-Diazoester to Access Phosphinic Hydrazone

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