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【结 构 式】

【分子编号】29152

【品名】ethyl 2-(5H-dibenzo[a,d]cyclohepten-5-ylidene)acetate

【CA登记号】

【 分 子 式 】C19H16O2

【 分 子 量 】276.33484

【元素组成】C 82.58% H 5.84% O 11.58%

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 Wittig condensation of triethyl phosphonoacetate (II) with 5H-dibenzo[a,d]cyclohepten-5-one (I) by means of NaH in DMSO gives the ethyl (III), which is finally hydrolyzed with KOH in refluxing ethanol.

1 Bergmann, E.D.; Solomonovici, A.; Fulvenes and thermochromic ethylenes. 57. Wittig-Homer reaction with fulvene ketones and related ketones. Synthesis 1970, 2, 4, 183-189.
2 Wolf, M. (American Home Products Corp.); Method for treating inflammation. EP 0035903; GB 2071098; JP 82500244; US 4267192 .
3 Serradell, M.N.; Castaner, J.; Arrigoni-Martelli, E.; WY-41770. Drugs Fut 1985, 10, 4, 309.
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) 29151 5H-dibenzo[a,d]cyclohepten-5-one; Dibenzosuberenone 2222-33-5 C15H10O 详情 详情
(II) 10019 Ethyl 2-(diethoxyphosphoryl)acetate; Triethyl phosphonoacetate 867-13-0 C8H17O5P 详情 详情
(III) 29152 ethyl 2-(5H-dibenzo[a,d]cyclohepten-5-ylidene)acetate C19H16O2 详情 详情
Extended Information