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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488192생성일: 2026년 10월 24일

Carbon Dioxide → Octyl isocyanate

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

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물OctylamineHCID 8143—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물TridecaneHCID 12388—
반응물Carbamic acid, octyl esterHCID 16240—
반응물2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
생성물Octyl isocyanateHCID 7661683%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05298651
출처 데이터셋uspto-grants-1994_03
ORD IDord-a94e07fb9bf144f8b25e2dbb9e528e37
출처 메모uspto-grants-1994_03