돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354598생성일: 2026년 10월 24일

Allyl chloride → Allyl chloride

https://huagongshe.com/ko/reaction/354598

반응식

참여 물질

역할이름HCID투입량
반응물Allyl chlorideHCID 7850—
반응물TriethylamineHCID 8471—
반응물Sodium CarbonateHCID 10340—
반응물Tetrabromophthalic anhydrideHCID 12443—
반응물Sodium HydroxideHCID 14798—
반응물SodiumHCID 5360545—
반응물HCID 20508441HCID 20508441—
용매Allyl AlcoholHCID 7858—
생성물Allyl chlorideHCID 7850—
생성물HCID 15376696HCID 15376696—

반응 단계

In the preferred embodiment of this invention for the production of DATBP, 1 mole of tetrabromophthalic anhydride, 0.55 mole of sodium carbonate (or 1 mole of sodium hydroxide) and a catalytic amount (0.024 mole) of triethylamine are added to a large excess (up to 10-20 moles) of allyl alcohol as a solvent as well as a reactant. If sodium hydroxide is used as the base, it is convenient to dissolve it in the allyl alcohol before the addition of the tetrabromophthalic anhydride. The mixture is stirred and heated to 90° C.-95° C. to speed the reaction to completion, yielding a solution or a thin suspension of the sodium salt of monoallyl tetrabromophthalate. After the completion of this step, 1.2 moles of allyl chloride plus a catalytic amount (0.33 mole) of allyltriethylammonium chloride (either preformed or formed in situ from triethylamine and additional allyl chloride) are added and the mixture is heated in a closed vessel for 2 hours at 100° C.-110° C., developing an equilibrium pressure of 103 kPa-172 kPa (15-25 psig). Longer heating may be required if no pressure is allowed to develop. On cooling, the DATBP crystallizes and the separated product requires only washing with cold water and drying to assay 94% to 98%. The washing may be accomplished by merely spraying with water in a centrifuge.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04375551
출처 데이터셋uspto-grants-1983_03
ORD IDord-c9922d6df8be44648d6627e93b082f7b
출처 메모uspto-grants-1983_03