돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1297573생성일: 2026년 10월 24일

Sulfuric Acid → Di-tert-amylcyclohexylphosphine

https://huagongshe.com/ko/reaction/1297573

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물ChlorocyclohexaneHCID 10952—
반응물MagnesiumHCID 5462224—
반응물Di-tert-amylphosphinous chlorideHCID 23032008—
촉매Cuprous chlorideHCID 62652—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물Di-tert-amylcyclohexylphosphineHCID 2292548196.7%

반응 단계

In a 300 ml four-necked flask thoroughly purged with nitrogen, 10.4 g (0.05 mol) of di-tert-amylphosphinous chloride, 0.10 g (0.001 mol (corresponding to 2% by mol)) of copper(I) chloride and 30 ml of tetrahydrofuran were placed. To the contents of the flask, a Grignard reagent solution previously prepared from 8.3 g (0.060 mol) of cyclohexyl chloride and 2.0 g (0.08 mol) of metallic magnesium in 50 ml of tetrahydrofuran was dropwise added over a period of 1 hour with maintaining the temperature at 25° C. to 30° C. After the dropwise addition was completed, stirring was conducted at a temperature of 35° C. to 40° C. for 6 hours. After the temperature of the reaction solution was returned to room temperature, 20 ml of toluene and 20 ml of a 5% sulfuric acid aqueous solution were added to the reaction solution to perform liquid separation. Then, the organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent and a low-boiling component were distilled off under reduced pressure to obtain 12.4 g (purity: 94.9%) of the aimed di-tert-amylcyclohexylphosphine as an oily substance. The yield was 90.2%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07250535B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-b131fcae618b4d9db60a8b5908619afd
출처 메모uspto-grants-2007_07