戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 488194作成日:2026年10月25日

Carbon Dioxide → Octyl isocyanate

https://huagongshe.com/reaction/488194

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物TrimethylamineHCID 1146—
反応物OctylamineHCID 8143—
反応物TridecaneHCID 12388—
反応物Carbamic acid, octyl esterHCID 16240—
反応物Methanamine, N,N-dimethyl-, compd. with sulfur trioxide (1:1)HCID 222852—
溶媒Diethyl EtherHCID 3283—
溶媒AcetonitrileHCID 6342—
生成物Octyl isocyanateHCID 7661611%

反応手順

A Fischer-Porter bottle was charged with 0.55 g (4.2 mmol) of octyl amine, 0.99 g of P1 tBu (3 mmol), 25 mL of acetonitrile and 130 mg (0.84 mmol) of tridecane as an internal standard. The bottle was pressurized to 80 psig with carbon dioxide and the solution was stirred for 30 min. at room temperature. A second Ficher-Porter bottle was charged with 0.65 g (4.7 mmol) of sulfur trioxide trimethylamine adduct (SO3 -NMe3) and 20 mL of acetonitrile then pressurized to 80 psig with CO2. The two solutions were cooled to 0° C. in an ice bath for 10 min after which time the octyl carbamate solution was added rapidly to the SO3 -NMe3 suspension. An aliquot was taken after five minutes and diluted with diethyl ether prior to G.C. analysis which indicated a yield of 11% octyl isocyanate. Further monitoring of the reaction progress over 48 hrs gave a maximum yield of 27% octyl isocyanate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05298651
出典データセットuspto-grants-1994_03
ORD IDord-f85167ad5c124e16af34afd972aed7d2
出典メモuspto-grants-1994_03