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【结 构 式】

【分子编号】33456

【品名】1-chloro-3-phenoxy-2-propanol

【CA登记号】

【 分 子 式 】C9H11ClO2

【 分 子 量 】186.63784

【元素组成】C 57.92% H 5.94% Cl 19% O 17.14%

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)

1) By condensation of phenol (I) with 1-n-butoxy-2,3-epoxypropane (VII) in presence of potassium hydroxide. 2) By condensation of phenol (I) with 1-chloro-2,3-epoxypropane (II) followed either by addition of n-butanol (VI) in presence of a Lewis acid or in presence of a base (IV).

1 Hoffmann, H.; et al.; Procedimiento de fabricacion de sustancias medicinalmente activas y metodo de preparacion de medicamentos de accion coleretica. ES 402799; FR 2134389; GB 1393451; US 3839587 .
2 Janiak, P. St.; Febuprol. Drugs Fut 1978, 3, 3, 191.
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) 23540 Phenol 108-95-2 C6H6O 详情 详情
(II) 10146 Epichlorohydrin; 2-(Chloromethyl)oxirane 106-89-8 C3H5ClO 详情 详情
(III) 33456 1-chloro-3-phenoxy-2-propanol C9H11ClO2 详情 详情
(IV) 33457 sodium 1-butanolate; Sodium butoxide; Sodium n-butoxide 2372-45-4 C4H9NaO 详情 详情
(V) 23932 2-(phenoxymethyl)oxirane; oxiranylmethyl phenyl ether 122-60-1 C9H10O2 详情 详情
(VI) 29766 butanol; n-butanol; 1-butanol 71-36-3 C4H10O 详情 详情
(VII) 33458 2-(butoxymethyl)oxirane; butyl 2-oxiranylmethyl ether 2426-08-6 C7H14O2 详情 详情
Extended Information