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HRID 2118921作成日:2026年10月24日

Pyridine → p-Nitrophenyl 5-benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylate

https://huagongshe.com/ja/reaction/2118921

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-Nitrophenyl trifluoroacetateHCID 69569—
反応物5-Benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylic acidHCID 13364578—
溶媒PentaneHCID 8003—
生成物p-Nitrophenyl 5-benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylateHCID 1336458080.2%

反応手順

A mixture of 3.3 g (7.53 mmole) 5-benzyloxy-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran-4-carboxylic acid, 5.0 g (21.3 mmole) p-nitrophenyl trifluoroacetate and 100 ml dry pyridine, under nitrogen, is stirred at room temperature for three hours. The pyridine is evaporated in vacuo, ethyl ether is added to the residue and this is washed with 1N sodium hydroxide, water, 10% hydrochloric acid, brine, dried (MgSO4) and the solvent evaporated to obtain 4.5 g crude oil. This is taken up in pentane and cooled to obtain 3.38 g of crystals, m.p. 87°-87.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04680404
出典データセットuspto-grants-1987_07
ORD IDord-c577b0a4d8c5405b8b1cdb10e169194f
出典メモuspto-grants-1987_07