戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1065212作成日:2026年10月25日

Water → 2,3-Dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamate

https://huagongshe.com/reaction/1065212

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物CarbofuranHCID 2566—
反応物TriethylamineHCID 8471—
反応物Amidosulfenyl chloride, N,N-dibutyl-HCID 81031—
触媒Triethylamine sulfur dioxideHCID 12824984—
溶媒HexaneHCID 8058—
生成物2,3-Dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamateHCID 1320639190%

反応条件

温度11 °C

反応手順

A flask was charged with 30.2 g of a 50% solution of dibutylaminosulfenyl chloride (0.077 mole) in hexane and 15.8 g of 98% 2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate (0.07 mole) was added. Triethylamine (7.8 g, 0.077 mole) was added to the mixture with agitation over a period of seven minutes. A temperature rise from 24.5° to 26° C. was observed. A portion (1.9 g, 0.0115 mole) of the triethylamine/sulfur dioxide catalyst prepared in Example 3 was added dropwise. The temperature gradually rose to 30° C., and was raised further by external heating to 35° C. for a total reaction time of 100 minutes from the beginning of triethylamine addition. Twenty minutes later the mixture was cooled to 11° C. and 31 ml of water was added and mixed. The mixture was filtered to remove a small amount of solid, separated, and the organic layer was concentrated to yield 26.64 g of 90% (hplc) 2,3-dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamate (a 90% chemical yield based on the starting carbamate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04329293
出典データセットuspto-grants-1982_05
ORD IDord-07ad1bb7582f4de9bbc9893b077fb3b8
出典メモuspto-grants-1982_05