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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 364761생성일: 2026년 10월 27일

Acetic Acid → 6-Chloromethyl-1,1,4,4,7-pentamethyl-5-methoxy-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/364761

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Phosphoric AcidHCID 1004—
반응물5-Methoxy-1,1,4,4,7-pentamethyl-1,2,3,4-tetrahydronaphthaleneHCID 226702—
용매BenzeneHCID 241—
생성물6-Chloromethyl-1,1,4,4,7-pentamethyl-5-methoxy-1,2,3,4-tetrahydronaphthaleneHCID 19095170—

반응 조건

온도95 °C

반응 단계

1-Methoxy-3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalene (23.2 g, 0.1 mol), prepared according to Example 2, was added to a stirred solution of acetic acid (18.2 g, 0.3 mol), 85% phosphoric acid (17.6 g, 0.15 mol), hydrochloric acid (28.7 g, 0.3 mol) and paraformaldehyde (7.3 g, 0.24 mol). The mixture was stirred and heated at 95° C. for 16 h. The reaction mixture was then cooled to 25° C., benzene (50 mL) added, and stirred vigorously. The organic layer was separated, washed with water (2×25 mL), neutralized with 5% sodium bicarbonate solution, and dried (Na2SO4). The solvent was removed by distillation to provide 2-chloromethyl-1-methoxy-3,5,5,8,8,-pentamethyl-5,6,7,8-tetrahydronaphthalene, GLC purity 84%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04605778
출처 데이터셋uspto-grants-1986_08
ORD IDord-c8687e61aa3448abbd6716af3118ebc1
출처 메모uspto-grants-1986_08