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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 408975생성일: 2026년 10월 25일

1-Naphthol → 1-Dichlorophosphoryloxynaphthalene

https://huagongshe.com/reaction/408975

반응식

참여 물질

역할이름HCID투입량
반응물1-NaphtholHCID 7005—
반응물TriethylamineHCID 8471—
반응물Phosphorus oxychlorideHCID 24813—
용매tert-Butyl methyl etherHCID 15413—
생성물1-DichlorophosphoryloxynaphthaleneHCID 57563186.3%

반응 단계

In a 22 L 3-neck flask equipped with a mechanical stirrer, an internal thermocouple, a cooling bath of dry/acetone, an additional funnel and a nitrogen inlet was placed 1-naphthol (780 g, 5.41 mol, 491 g used from Aldrich, ≧99% grade, Product No N1000 and 289 g used from Alfa Aesar 99% grade, Product No A11862) in 10 L of MTBE at room temperature. POCl3 (495 mL, 5.41 mol, ReagentPlus® 99%, Product No 201170, Aldrich) in an additional funnel was dropwise added in 5 min (note: no exothermic observed) under nitrogen pressure. To this solution at −25° C. (an internal temperature) was slowly added by triethylamine (754 mL, 5.41 mol, ≧99.5% grade, Product No 471283, Aldrich) for one h (note: exotherm observed) and then the cooling bath was removed after the addition was completed. The reaction mixture was aged for 3 h at room temperature under nitrogen pressure. The triethylamine hydrochloride salt was filtered off using a 3 L sintered funnel (Medium size) and the filtrate was concentrated to dryness under reduced pressure at <20° C. of water bath to give desired product as clear dark yellow oil (1219 g, 86.3%) which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759318B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-7dbfc56f4ed540c6bbe39e72afc5b556
출처 메모uspto-grants-2014_06