8-(Benzyloxy)-3,4-dihydronaphthalen-1(2H)-one

Base Information

• Chemical Name: 8-(Benzyloxy)-3,4-dihydronaphthalen-1(2H)-one
• CAS No.: 88058-45-1
• Molecular Formula: C17H16O2
• Molecular Weight: 252.313
• Hs Code.: 2914509090
• DSSTox Substance ID: DTXSID00540754
• Wikidata: Q82416864
• Mol file: 88058-45-1.mol

Synonyms:8-(Benzyloxy)-3,4-dihydronaphthalen-1(2H)-one;88058-45-1;8-phenylmethoxy-3,4-dihydro-2H-naphthalen-1-one;SCHEMBL7280823;DTXSID00540754

Chemical Property of 8-(Benzyloxy)-3,4-dihydronaphthalen-1(2H)-one

Chemical Property:

• PSA: 26.30000
• LogP: 3.78460
• Storage Temp.: 2-8°C
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 252.115029749
• Heavy Atom Count: 19
• Complexity: 306

Purity/Quality:

≥99% ^*data from raw suppliers

8-(Benzyloxy)-3,4-dihydronaphthalen-1(2H)-one 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC2=C(C(=O)C1)C(=CC=C2)OCC3=CC=CC=C3

Technology Process of 8-(Benzyloxy)-3,4-dihydronaphthalen-1(2H)-one

There total 2 articles about 8-(Benzyloxy)-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:

Reference yield: 93.0%

8-hydroxy-1,2,3,4-tetrahydro-1-naphthalenone (7695-47-8) + benzyl chloride (100-44-7) → 8-benzyloxy-1,2,3,4-tetrahydro-1-naphthalenone (88058-45-1)

Guidance literature:

With potassium phosphate; In dimethyl sulfoxide; at 60 ℃; for 0.333333h;

DOI:10.1002/jhet.5570330104

Reference yield: 71.0%

8-hydroxy-1,2,3,4-tetrahydro-1-naphthalenone (7695-47-8) + benzyl bromide (100-39-0) → 8-benzyloxy-1,2,3,4-tetrahydro-1-naphthalenone (88058-45-1)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 70 ℃; for 4h;

DOI:10.1021/jacs.8b05724

Reference yield:

1,4-dibromo-butane (110-52-1) + 8-benzyloxy-1,2,3,4-tetrahydro-1-naphthalenone (88058-45-1) → 8'-benzyloxy-3'4'-dihydro-spiro[cyclopentane-1,2'(1'H)-naphthalen]-1'-one (162180-26-9)

Guidance literature:

With potassium tert-butylate; In tetrahydrofuran; water;

upstream raw materials:

8-hydroxy-1,2,3,4-tetrahydro-1-naphthalenone

benzyl chloride

benzyl bromide

Downstream raw materials:

2-phenyl-4,5-dihydro-3H-naphtho<1,8-bc>furan

8-(1-hydroxy-1-phenylmethyl)-1,2,3,4-tetrahydro-1-naphthalenone

8-Benzyloxy-3,4-dihydro-[1,2]naphthoquinone 2-oxime

10-Phenylmethoxy-5,6-dihydrobenzo[h]cinnolin-3(2H)-one

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