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【结 构 式】

【分子编号】39585

【品名】6-[(Z,2Z)-3-methoxy-2-butenylidene]-1,5,5-trimethyl-1-cyclohexene; methyl (Z)-1-methyl-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-propenyl ether

【CA登记号】

【 分 子 式 】C14H22O

【 分 子 量 】206.32808

【元素组成】C 81.5% H 10.75% O 7.75%

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:(XI)

The reaction of beta-ionon (X) with triethyl orthoformate (A) by means of H2SO4 in dioxane gives beta-ionon enolether (XI), which by reaction with NBS in CCl4 and hydrolysis with acetic acid is converted into 4-acetoxyonon (XII). The Grignard reaction of (XII) with vinylmagnesium bromide (B) in THF and hydrolysis with KOH in methanol gives 5-(3-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3-methylpenta-1,4-dien-3-ol (XIII), which is oxidized with MnO2 in methylene chloride yielding 5-(3-oxo-2,6,6-trimethylcyclohex-1-en-1-yl)-3-methylpenta-1,4-dien-3-ol (XIV). Finally, this compound by reaction with triphenylphosphonium bromide (C) in DMF is converted into the phosphonium salt (VIII), which is finally condensed in a Wittig reaction with 2,7-dimethyl-2,4,6-octatriene-1,8-dial (IX) by means of sodium methoxide in dichloromethane.

1 Rosenberg, M.; US 4000198 .
2 Serradell, M.N.; Blancafort, P.; Castaner, J.; Hillier, K.; Canthazanthin. Drugs Fut 1979, 4, 7, 477.
3 Rigassi, N.; Schwieter, U.; DE 2037935 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(B) 16524 bromo(vinyl)magnesium 1826-67-1 C2H3BrMg 详情 详情
(A) 21304 Triethyl orthoformate; 1-(Diethoxymethoxy)ethane; Diethoxymethyl ethyl ether 122-51-0 C7H16O3 详情 详情
(VIII) 39582 [(2E,4E)-3-methyl-5-(2,6,6-trimethyl-3-oxo-1-cyclohexen-1-yl)-2,4-pentadienyl](triphenyl)phosphonium bromide C33H36BrOP 详情 详情
(IX) 39583 (2E,4E,6E)-2,7-dimethyl-2,4,6-octatrienedial C10H12O2 详情 详情
(X) 39584 (E)-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one 14901-07-6 C13H20O 详情 详情
(XI) 39585 6-[(Z,2Z)-3-methoxy-2-butenylidene]-1,5,5-trimethyl-1-cyclohexene; methyl (Z)-1-methyl-3-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-1-propenyl ether C14H22O 详情 详情
(XII) 39586 2,4,4-trimethyl-3-[(E)-3-oxo-1-butenyl]-2-cyclohexen-1-yl acetate C15H22O3 详情 详情
(XIII) 39587 3-[(1E)-3-hydroxy-3-methyl-1,4-pentadienyl]-2,4,4-trimethyl-2-cyclohexen-1-ol C15H24O2 详情 详情
(XIV) 39588 3-[(1E)-3-hydroxy-3-methyl-1,4-pentadienyl]-2,4,4-trimethyl-2-cyclohexen-1-one C15H22O2 详情 详情
(C) 39589 triphenylphosphonium bromide 6399-81-1 C18H16BrP 详情 详情
Extended Information