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HRID 1856435생성일: 2026년 10월 26일

Hydrochloric Acid → 3-Chloro-2-phenyloxane

https://huagongshe.com/reaction/1856435

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물BromobenzeneHCID 7961—
반응물2,3-DichlorotetrahydropyranHCID 529964—
용매Diethyl EtherHCID 3283—
생성물3-Chloro-2-phenyloxaneHCID 24361593%

반응 단계

Into a dry flask fitted with dropping funnel reflux condenser, drying tube and mechanical stirrer was placed 51 g of magnesium turnings, followed by the addition of 200 ml of dry ether. A small portion of bromobenzene was added to initiate the reaction, followed by the remainder of 330 g (2.1 mole) of bromobenzene in 1 liter of dry ether at a rate sufficient to maintain reflux. The mixture was cooled in an ice-salt bath to which was added dropwise the cold ethereal solution of 2,3-dichlorotetrahydropyran. After completing the addition, the slurry was refluxed for 3 hours, cooled in an ice-water bath and 300 ml of cold 20 percent hydrochloric acid added slowly to the stirred mixture. The addition of 500 ml of water dissolved the precipitated salts, the layers were separated, the aqueous phase extracted with ether (2×200 ml) and the combined ethereal layers washed with brine (200 ml) and dried over anhydrous potassium carbonate. In vacuo removal of solvent left an amber liquid which was distilled through a 20 cm Vigreux column, whereby 256 g was collected at 77°-90°/0.25 mm Hg. The product was redistilled at 153-154/16 mm Hg, the distillate crystallizing to give needles m.p. 39.5°-40.5°. The crude yield was 256 g (93% yield based on dihydropyran).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04219489
출처 데이터셋uspto-grants-1980_08
ORD IDord-a43635adfb6747389e67242a49ac91d4
출처 메모uspto-grants-1980_08