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【结 构 式】

【分子编号】51335

【品名】2-methyloctanoyl chloride

【CA登记号】

【 分 子 式 】C9H17ClO

【 分 子 量 】176.68608

【元素组成】C 61.18% H 9.7% Cl 20.07% O 9.06%

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 dilithium anion of octanoic acid (I) was alkylated with iodomethane in the presence of HMPA to afford 2-methyloctanoic acid (II). After conversion of (II) to the corresponding acid chloride (III), condensation with (-)-epigallocatechin (IV) using trifluoroacetic acid as the catalyst furnished the title 3-O-acyl epigallocatechin.

1 Uesato, S.; et al.; Antitumor promoting activities of 3-O-acyl-(-)-epigallocatechins. Bioorg Med Chem Lett 2000, 10, 15, 1673.
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) 11091 Octanoic acid 124-07-2 C8H16O2 详情 详情
(II) 51334 2-Methyloctanoic acid C9H18O2 详情 详情
(III) 51335 2-methyloctanoyl chloride C9H17ClO 详情 详情
(IV) 51336 (2R,3R)-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol C15H14O7 详情 详情
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