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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334191생성일: 2026년 10월 24일

Phenol → Phenyl cyanate

https://huagongshe.com/ko/reaction/334191

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물PentaneHCID 8003—
반응물Cyanogen BromideHCID 10476—
용매Diethyl EtherHCID 3283—
용매TriethylamineHCID 8471—
생성물Phenyl cyanateHCID 70740—

반응 단계

To a oven dried 500 mL 3-neck round bottom flask equipped with a overhead stirring, a septa, a thermocouple and the nitrogen inlet, phenol (20.0 g, 0.210 mol), diethyl ether (Et2O, 290 mL) and cyanic bromide (BrCN, 23.0 g, 0.210 mol, 1.0 equiv) were added at room temperature. The resulting solution was cooled down to 0-3° C. before triethylamine (TEA, 61.9 mL, 0.442 mol, 2.1 equiv) was added dropwise via syringe over 25 min. The addition of triethylamine to reaction mixture was mildly exothermic and the reaction temperature went up to as high as 15° C. After addition of triethylamine, the reaction mixture became a white slurry which was stirred vigorously at 0° C. for 2 h at 5-15° C. When the reaction was deemed complete as confirmed by TLC and LCMS, the reaction mixture was diluted with pentane (150 mL, 1.30 mol). The precipitated triethylamine hydrochloride was filtered off and the salt was washed with diethyl ether and pentane (1 to 1 by volume, 200 mL). The filtrate was then concentrated under reduced pressure to remove the majority of the solvent, and the residue, which contains the crude cyanatobenzene (6), was directly used in the subsequent reaction without further purification assuming the theoretical yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883806B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-1e9ef0b8654e47b88052325369b5241b
출처 메모uspto-grants-2014_11