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HRID 2052453作成日:2026年10月26日

1,3,6-Naphthalenetrisulfonic acid, 8-amino-, sodium salt (1:?) → 8-(4-Nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium salt

https://huagongshe.com/reaction/2052453

反応式

関与物質

役割名称HCID仕込み量
反応物1,3,6-Naphthalenetrisulfonic acid, 8-amino-, sodium salt (1:?)HCID 101899—
反応物Sodium Acetate TrihydrateHCID 23665404—
反応物4-Nitro-2-sulfobenzoic anhydrideHCID 57002923—
溶媒WaterHCID 962—
生成物8-(4-Nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium saltHCID 131711368296.2%

反応手順

To an ice bath cooled solution (5° C.) of 16.0 g of 8-amino-1,3,6-naphthalenetrisulfonic acid trisodium salt and 6.7 g of sodium acetate trihydrate in 100 ml of water is added 8.8 g of 4-nitro-2-sulfobenzoic acid anhydride. The mixture is stirred vigorously for 10 minutes and is filtered. The filtrate is cooled in an ice bath and diluted with 500 ml of cold ethanol. The mixture is filtered and the product is washed with ethanol and ether and then is dried. The product is dissolved in 50 ml of warm water and is stirred for 10 minutes after the addition of one ml of acetone. The mixture is treated with activated charcoal, filtered through diatomaceous earth and is washed with 20 ml of water. The filtrate is cooled in an ice bath and acidified with 1.5 ml of concentrated hydrochloric acid. The solution is diluted with 500 ml of cold ethanol and the precipitated material is filtered, washed with ethanol followed by ether and dried. The above purification process is repeated without acidification. The product obtained is dried overnight at 110° C. to give 18.5 g of 8-(4-nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04185032
出典データセットuspto-grants-1980_01
ORD IDord-52af5f890a374cc6ba0e14acca3948bf
出典メモuspto-grants-1980_01