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7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one

Base Information
  • Chemical Name:7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one
  • CAS No.:79754-58-8
  • Molecular Formula:C17H16O3
  • Molecular Weight:268.312
  • Hs Code.:
7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one

Synonyms:7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one

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Chemical Property of 7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one
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Technology Process of 7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one

There total 17 articles about 7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogen bromide; In acetic acid; for 6h; Heating;
DOI:10.1039/P19810002662
Guidance literature:
Multi-step reaction with 5 steps
1: 21 percent / dry hydrogen chloride / tin(II) chloride / diethyl ether / 6 h
2: 20 percent / piperidine / pyridine / 1.) steam-bath, 10 h, 2.) reflux, 4 h
3: 63 percent / aq. sodium hydroxide, nickel-aluminium alloy / 2 h / 80 °C
4: 84 percent / polyphosphoric acid / 1.5 h / 85 °C
5: 76 percent / 48percent hydrobromic acid / acetic acid / 6 h / Heating
With piperidine; hydrogenchloride; sodium hydroxide; PPA; nickel-aluminium alloy; hydrogen bromide; tin(ll) chloride; In pyridine; diethyl ether; acetic acid;
DOI:10.1039/P19810002662
Guidance literature:
Multi-step reaction with 7 steps
1: perchloric acid, hydrogen / 10percent palladium-carbon / acetic acid / 17 h / 735.5 Torr
2: ethanolic potassium hydroxide / H2O
3: thionyl chloride
4: diethyl ether / 0 °C
5: silver oxide, aq. sodium thiosulphate / dioxane / 2 h / 65 - 70 °C
6: 84 percent / polyphosphoric acid / 1.5 h / 85 °C
7: 76 percent / 48percent hydrobromic acid / acetic acid / 6 h / Heating
With potassium hydroxide; thionyl chloride; perchloric acid; PPA; hydrogen bromide; hydrogen; sodium thiosulfate; silver(l) oxide; palladium on activated charcoal; In 1,4-dioxane; diethyl ether; water; acetic acid;
DOI:10.1039/P19810002662
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