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【结 构 式】

【分子编号】46056

【品名】bromo(6-methoxy-2-naphthyl)magnesium

【CA登记号】

【 分 子 式 】C11H9BrMgO

【 分 子 量 】261.40086

【元素组成】C 50.54% H 3.47% Br 30.57% Mg 9.3% O 6.12%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VII)

By condensation of 2-bromo-6-methoxynaphthalene (I) with 3-buten-2-ol (VI) catalyzed by Pd(OAc)2 or PdCl2, along with PPh3 and NaHCO3 in 1-methyl-2-pyrrolidone at 140 C. The reaction of 2-bromo-6-methoxynaphthalene (I) with Mg in THF gives the expected Grignard reagent (VII), which is then condensed with 3-buten-2-one (II) by means of ZnCl2-amine complex in the same solvent.

1 Aslam, M.; et al.; Convenient synthesis of nabumetone. Synthesis 1989, 869.
2 Wang, S.-M.; Chen, Z.-X.; Novel synthesis of nabumetone. Chin J Pharm 1989, 20, 4, 146.
3 Davenport, K.G.; Aslam, M. (Celanese AG); Method of preparation of nabumetone. EP 0376516 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 44399 2-bromo-6-methoxynaphthalene; 6-bromo-2-naphthyl methyl ether 5111-65-9 C11H9BrO 详情 详情
(II) 30324 3-buten-2-one; methyl vinyl ketone 78-94-4 C4H6O 详情 详情
(VI) 46055 3-buten-2-ol C4H8O 详情 详情
(VII) 46056 bromo(6-methoxy-2-naphthyl)magnesium C11H9BrMgO 详情 详情
Extended Information