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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488194생성일: 2026년 10월 24일

Carbon Dioxide → Octyl isocyanate

https://huagongshe.com/ko/reaction/488194

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물TrimethylamineHCID 1146—
반응물OctylamineHCID 8143—
반응물TridecaneHCID 12388—
반응물Carbamic acid, octyl esterHCID 16240—
반응물Methanamine, N,N-dimethyl-, compd. with sulfur trioxide (1:1)HCID 222852—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
생성물Octyl isocyanateHCID 7661611%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05298651
출처 데이터셋uspto-grants-1994_03
ORD IDord-f85167ad5c124e16af34afd972aed7d2
출처 메모uspto-grants-1994_03