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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2269658생성일: 2026년 10월 25일

Hydrochloric Acid → 2-Chloro-6-fluorobenzene-1-carbothioamide

https://huagongshe.com/reaction/2269658

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물2-Chloro-6-fluorobenzonitrileHCID 69587—
반응물Sodium sulfide monohydrateHCID 19906495—
용매PyridineHCID 1049—
생성물2-Chloro-6-fluorobenzene-1-carbothioamideHCID 7745242—

반응 단계

Into a 250-mL three necked round bottom flask equipped with a mechanical stirrer, dry ice condenser, dropping funnel, and outlet to a trap filled with bleach was added pyridine (45 mL), 2-chloro-6-fluorobenzonitrile (15.5 g, 0.1 mol), triethylamine (13.4 g, 18.6 mL, 0.133 mol), and sodium sulfide hydrate (36.0 g, 0.15 mol). The temperature of the resulting solution was lowered to approximately 5° C. using an ice bath. To the stirred slurry was added dropwise concentrated hydrochloric acid (25.8 g, 0.266 mol). The rate of addition of the hydrochloric acid was such that the temperature of the reaction mixture did not exceed 25° C. with an addition time of 20 min. The cooling bath was removed and the slurry was allowed to warm to RT and to stir over night. An additional 40 grams of sodium sulfide and 50 mL of hydrochloric acid was added to the mixture and allowed to stir over night. An additional 40 grams of sodium sulfide and 50 mL of hydrochloric acid was added and the mixture allowed to stir over the weekend. The mixture was poured into water (2 L) and was extracted with ether. The ether layer was washed with dilute sulfuric acid, water, brine, dried (MgSO4), and the solvent removed in vacuo to give 16.1 g of crude product which was recrystallized from ethyl acetate to give 2-chloro-6-fluoro-benzthioamide as light yellow crystals: mp 156-158° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06329528B1
출처 데이터셋uspto-grants-2001_12
ORD IDord-e95fcdd4b44d42b194ba493fd06d6e62
출처 메모uspto-grants-2001_12