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【结 构 式】

【分子编号】67298

【品名】(S)-2-((S)-6-fluorochroman-2-yl)-2-hydroxyethyl benzoate

【CA登记号】 

【 分 子 式 】C18H17FO4

【 分 子 量 】316.329

【元素组成】C 68.34% H 5.42% F 6.01% O 20.23%

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:(XV)

 

1 余婧,张稳稳,李映红,等.2008.奈必洛尔的不对称合成.有机化学,28(3):511~514
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) 19639 4-fluorophenol 371-41-5 C6H5FO 详情 详情
(II) 40848 1-(allyloxy)-4-fluorobenzene; allyl 4-fluorophenyl ether C9H9FO 详情 详情
(III) 40849 2-allyl-4-fluorophenol C9H9FO 详情 详情
(IV) 40850 (2-allyl-4-fluorophenoxy)(tert-butyl)dimethylsilane; 2-allyl-4-fluorophenyl tert-butyl(dimethyl)silyl ether C15H23FOSi 详情 详情
(V) 40851 3-(2-[[tert-butyl(dimethyl)silyl]oxy]-5-fluorophenyl)-1-propanol C15H25FO2Si 详情 详情
(VI) 40852 3-(2-[[tert-butyl(dimethyl)silyl]oxy]-5-fluorophenyl)propanal C15H23FO2Si 详情 详情
(VII) 40853 ethyl (E)-5-(2-[[tert-butyl(dimethyl)silyl]oxy]-5-fluorophenyl)-2-pentenoate C19H29FO3Si 详情 详情
(VIII) 40854 (E)-5-(2-[[tert-butyl(dimethyl)silyl]oxy]-5-fluorophenyl)-2-penten-1-ol C17H27FO2Si 详情 详情
(IX) 40855 4-fluoro-2-[(E)-5-hydroxy-3-pentenyl]phenol C11H13FO2 详情 详情
(X) 40856 (1R)-1-[(2S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl]-1,2-ethanediol C11H13FO3 详情 详情
(XI) 40857 (2R)-2-[(2S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl]-2-hydroxyethyl 4-methylbenzenesulfonate C18H19FO5S 详情 详情
(XII) 40858 (1R)-2-azido-1-[(2S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl]-1-ethanol C11H12FN3O2 详情 详情
(XIII) 40859 (1R)-2-amino-1-[(2S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl]-1-ethanol C11H14FNO2 详情 详情
(XIV) 67297 (1S)-1-[(2S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl]-1,2-ethanediol   C11H13FO3 详情 详情
(XV) 67298 (S)-2-((S)-6-fluorochroman-2-yl)-2-hydroxyethyl benzoate   C18H17FO4 详情 详情
(XVI) 67299 (S)-2-((S)-6-fluorochroman-2-yl)-2-(tosyloxy)ethyl benzoate   C25H23FO6S 详情 详情
(XVII) 67300 (R)-6-fluoro-2-((R)-oxiran-2-yl)chroman   C11H11FO2 详情 详情
Extended Information