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【结 构 式】

【分子编号】14587

【品名】(3-Bromophenyl)(trimethyl)silane; (3-Bromophenyl)trimethylsilane

【CA登记号】17878-47-6

【 分 子 式 】C9H13BrSi

【 分 子 量 】229.19172

【元素组成】C 47.17% H 5.72% Br 34.86% Si 12.25%

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:(III)

The reaction of 1,3-dibromobenzene (I) with trimethylsilyl chloride (II) by means of Mg in ethyl ether gives 3-(trimethylsilyl)bromobenzene (III), which is then condensed with ethyl trifluoroacetate (IV) by means of butyllithium in ethyl ether - hexane.

1 Schirlin, D.; Collard, J.-N.; Hornsperger, J.-M. (Merrell Pharmaceuticals, Inc.); Novel acetylcholinesterase inhibitors. EP 0403713; EP 0409676; JP 1991038591; US 5693668 .
2 Prous, J.; Graul, A.; Castaner, J.; Subreum. Drugs Fut 1994, 19, 9, 845.
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) 13370 1,3-Dibromobenzene 108-36-1 C6H4Br2 详情 详情
(III) 14587 (3-Bromophenyl)(trimethyl)silane; (3-Bromophenyl)trimethylsilane 17878-47-6 C9H13BrSi 详情 详情
(IV) 14588 Ethyl 2,2,2-trifluoroacetate; Trifluoroethyl acetate 383-63-1 C4H5F3O2 详情 详情
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