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HRID 488192作成日:2026年10月23日

Carbon Dioxide → Octyl isocyanate

https://huagongshe.com/ja/reaction/488192

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OctylamineHCID 8143—
反応物Trifluoroacetic anhydrideHCID 9845—
反応物TridecaneHCID 12388—
反応物Carbamic acid, octyl esterHCID 16240—
反応物2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
溶媒Diethyl EtherHCID 3283—
溶媒AcetonitrileHCID 6342—
生成物Octyl isocyanateHCID 7661683%

反応手順

A Fischer-Porter bottle was charged with 0.65 g (5 mmol) of octyl amine, 2.74 g of BEMP (10 mmol), 25 mL of acetonitrile and 184 mg (1 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 Fischer-Porter bottle was charged with 0.71 mL (5 mmol) of trifluoroacetic anhydride and 25 mL of acetonitrile then pressurized to 80 psig with CO2. The two solutions were cooled to 0° C. in an ice bath for 10 minutes after which time the octyl carbamate solution was added rapidly to the trifluoroacetic anhydride solution. An aliquot was taken after five minutes and diluted with diethyl ether prior to G.C. analysis which indicated a yield of 83% octyl isocyanate. The reaction mixture was allowed to warm slowly to room temperature and aliquots were taken periodically for G.C. analysis. A maximum yield of 85% octyl isocyanate was obtained after ca. 30 minutes.

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-a94e07fb9bf144f8b25e2dbb9e528e37
出典メモuspto-grants-1994_03