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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 625896생성일: 2026년 10월 24일

Azobisisobutyronitrile → HCID 90238913, 화합물

https://huagongshe.com/ko/reaction/625896

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물TriethylamineHCID 8471—
반응물N-bromobutanimideHCID 67184—
반응물6-Chloro-1-indanoneHCID 5100705—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물HCID 90238913HCID 90238913—

반응 단계

To a solution of 6-chloro-1-indanone (II) (100.0 g, 600.2 mmol) in 1,2-dichloroethane (1.00 L) was added 2,2′-azo-bis-isobutyronitrile (9.86 g, 60.0 mmol) followed by N-bromosuccinimide (224.3 g, 1.26 mol). The reaction mixture was quickly heated to reflux. After 30 min at reflux, more 2,2′-azo-bis-isobutyronitrile (9.86 g, 60.0 mmol) was added. The reaction mixture was kept for 4.5 h at reflux. Afterwards the mixture was stirred at room temperature overnight. The mixture was cooled to 0° C., and triethylamine (126 mL, 904 mmol) was added dropwise. The mixture was stirred for 1 h at 0° C., and then allowed to heat to room temperature. Water (1.0 L) was added. The mixture was vigorously stirred for 15 min. The stirring was stopped, and the aqueous layer was removed by suction. Fresh water (1.0 L) was added, and the mixture was stirred for 15 min. The aqueous layer was then separated by suction. The organic phase was further shaken with brine (500 mL) in a separating funnel.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309165B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-26fc7dc60172410ab7deafcb0da71c26
출처 메모uspto-grants-2016_04