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HRID 402972생성일: 2026년 10월 24일

Hydrochloric Acid → 1-(3-(Chloromethyl)phenyl)-2-hydroxy-2-methylpropan-1-one

https://huagongshe.com/ko/reaction/402972

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Sodium HydroxideHCID 14798—
반응물2-Hydroxy-2-methyl-1-phenylpropan-1-oneHCID 81984—
반응물Aluminum(III) ChlorideHCID 6451240—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물1-(3-(Chloromethyl)phenyl)-2-hydroxy-2-methylpropan-1-oneHCID 8669378933%

반응 조건

온도4 °C

반응 단계

under nitrogen atmosphere 5 grams of Darocur 1173 (2-hydroxy-2-methyl-1-phenylpropan-1-one) was mixed with 24 grams of anhydrous AlCl3 in 100 mL of dry chloroform. Upon cooling to 4° C. 4.5 grams of paraformaldehyde powder was slowly added and the resultant mixture was stirred at room temperature for 12 hrs (note that HCl gas released from the reaction was neutralized by 2N NaOH solution). The mixture was poured into water, and the precipitate generated was dissolved by adding 2N HCl solution. The organic layer thus separated was collected, and the aqueous layer was extracted with ethyl acetate for three times. The combined chloroform and ethyl acetate layer was next dried over anhydrous Na2SO4, filtered, and concentrated. The residue was loaded onto silica gel column and eluted by mixtures of hexane/ethyl acetate (V/V=15/1) to give the intermediate 1-(3-(chloromethyl)phenyl)-2-hydroxy-2-methylpropan-1-one as a light-yellow oil (33% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08742175B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-61a130eaae824248a8fd964ff58c0a7c
출처 메모uspto-grants-2014_06