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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290040생성일: 2026년 10월 27일

Methylparaben → 4-(2-Piperidinoethoxy)benzoic acid hydrochloride

https://huagongshe.com/reaction/1290040

반응식

참여 물질

역할이름HCID투입량
반응물MethylparabenHCID 7456—
반응물Potassium CarbonateHCID 11430—
반응물Piperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
용매Amyl AcetateHCID 12348—
생성물4-(2-Piperidinoethoxy)benzoic acid hydrochlorideHCID 574383591%

반응 단계

To a 2000 gallon tank were added: 1320 L of amyl acetate, 167.42 kg of methyl 4-hydroxybenzoate, 408.6 kg of potassium carbonate, and 283.5 kg of β-chloroethylpiperidine hydrochloride. The mixture was heated to 120° C.-125° C. for 5 hours, at which time HPLC analysis indicated complete consumption of the methyl 4-hydroxybenzoate. The tank was cooled to less than 50° C. 880 L of deionized water were added to the tank. The layers were separated and the aqueous layer was discarded. In a glass lined tank was mixed 367 L of food grade hydrochloric acid and 184 L of deionized water. The acid mixture was combined with the organic layer. The layers were separated and the organic layer was discarded. The mixture of the intermediate ester in aqueous acid heated to reflux until HPLC suggested no further consumption of the ester (13 hours). The mixture was cooled to less than 40° C. 550 L of acetone was added to the mixture and the mixture was cooled to 0° C.-5° C. and stirred for 1 hour. The product was collected by filtration on a centrifuge. The wet cake was rinsed on the centrifuge with 400 L of acetone. The product was dried in a rotary vacuum (double cone) dryer at less than 500 C and 25-27 inches in mercury. Yield was 91% of theoretical.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05750688
출처 데이터셋uspto-grants-1998_05
ORD IDord-33d51ac9f3a14264802aea2208a4a505
출처 메모uspto-grants-1998_05