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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1065556생성일: 2026년 10월 27일

Hydrochloric Acid → [1,1'-Biphenyl]-3-methanol, 2-methyl-

https://huagongshe.com/reaction/1065556

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium HydroxideHCID 14797—
반응물2-Methyl-3-nitrobenzyl alcoholHCID 90289—
촉매IronHCID 23925—
용매EthanolHCID 702—
생성물[1,1'-Biphenyl]-3-methanol, 2-methyl-HCID 596875—
생성물(3-Amino-2-methylphenyl)methanol hydrochlorideHCID 20270659—

반응 단계

2-Methyl[1,1'-biphenyl]-3-methanol was prepared as follows: To 100 ml of stirred 50% aqueous ethanol was added 2-methyl-3-nitrobenzyl alcohol (41.8 g, 0.25 mole) and 85.0 grams of iron powder. The mixture was brought to reflux, and 5.2 ml of concentrated hydrochloric acid was slowly added. Upon complete addition, the reaction mixture was stirred under reflux for 2 hours. The reaction mixture was then made just basic with ethanolic 15% potassium hydroxide. The hot mixture was filtered through diactomaceous earth to remove the iron. The filter cake was washed with ethanol. The filtrate was acidified with hydrogen chloride, then allowed to stand at room temperature for 16 hours. The ethanol was removed by evaporation under reduced pressure. Hexane was added to the residue, and the water-hexane azeotrope was removed by distillation. The addition of hexane and the subsequent removal of the water-hexane azeotrope by distillation was repeated three times. The 3-hydroxymethyl-2-methylaniline hydrochloride residue thus obtained was used as follows.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04329518
출처 데이터셋uspto-grants-1982_05
ORD IDord-d86913fc311c4f90af08a9f9532b4fa1
출처 메모uspto-grants-1982_05