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HRID 1607464作成日:2026年10月26日

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

https://huagongshe.com/reaction/1607464

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US04863934
出典データセットuspto-grants-1989_09
ORD IDord-15d1ff6694844b07be1afe178da2cc91
出典メモuspto-grants-1989_09