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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486419생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/486419

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Phosphoric AcidHCID 1004—
반응물2-Naphthalenecarboxaldehyde, 5,6,7,8-tetrahydro-1-methoxy-3,5,5,8,8-pentamethyl-HCID 174766—
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

To prepare the corresponding 6-carboxaldehyde, 6-formyl-1,1,4,4,7-pentamethyl-5-methoxy-1,2,3,4-tetrahydronaphthalene, 1,1,4,4,7-pentamethyl-5-methoxy-1,2,3,4-tetrahydronaphthalene (23.2 g, 0.1 mol) is 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 is stirred and heated at 95° C. for 16 hr. The reaction mixture is then cooled to 25° C., benzene (50 ml) added, and stirred vigorously. The organic layer is separated, washed with water (2×25 ml), neutralized with 5% sodium bicarbonate solution, and dried (Na2SO4). The solvent is removed by distillation to provide 6-chloromethyl-1,1,4,4,7-pentamethyl-5-methoxy-1,2,3,4-tetrahydronaphthalene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292719
출처 데이터셋uspto-grants-1994_03
ORD IDord-b855dfe161b34b50b9fc74599a97f95a
출처 메모uspto-grants-1994_03