2,3-Dihydro-6-(phenylmethoxy)-1H-inden-5-ol

Base Information

Chemical Name:2,3-Dihydro-6-(phenylmethoxy)-1H-inden-5-ol
CAS No.:83802-74-8
Molecular Formula:C₁₆H₁₆O₂
Molecular Weight:240.302
Hs Code.:
DSSTox Substance ID:DTXSID801262532

Synonyms:2,3-Dihydro-6-(phenylmethoxy)-1H-inden-5-ol;83802-74-8;DTXSID801262532

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2,3-Dihydro-6-(phenylmethoxy)-1H-inden-5-ol

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:240.115029749
Heavy Atom Count:18
Complexity:260

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2=CC(=C(C=C2C1)OCC3=CC=CC=C3)O

Technology Process of 2,3-Dihydro-6-(phenylmethoxy)-1H-inden-5-ol

There total 3 articles about 2,3-Dihydro-6-(phenylmethoxy)-1H-inden-5-ol 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:

Reference yield: 32.0%

: 3598-20-7
2,3-dihydro-1H-indene-5,6-diol

: 100-39-0
benzyl bromide

: 83802-74-8
5-(benzyloxy)-6-indanol

Guidance literature:: With sodium ethanolate; for 6h; Ambient temperature;
DOI:10.1021/jm00356a024

Reference yield:

: 2107-69-9
5,6-dimethoxy-1-indanone

: 83802-74-8
5-(benzyloxy)-6-indanol

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / Hg-Zn, concd. HCl / H₂O; toluene / 6 h / Heating

2: BBr₃ / CH₂Cl₂ / 3 h / 0 - 20 °C

3: 32 percent / 1.6 N NaOEt / 6 h / Ambient temperature

With hydrogenchloride; sodium ethanolate; boron tribromide; mercury; zinc; In dichloromethane; water; toluene;
DOI:10.1021/jm00356a024

Reference yield:

: 59078-28-3
5,6-dimethoxyindane

: 83802-74-8
5-(benzyloxy)-6-indanol

Guidance literature:: Multi-step reaction with 2 steps

1: BBr₃ / CH₂Cl₂ / 3 h / 0 - 20 °C

2: 32 percent / 1.6 N NaOEt / 6 h / Ambient temperature

With sodium ethanolate; boron tribromide; In dichloromethane;
DOI:10.1021/jm00356a024