2-Propanol, 1-(phenylmethoxy)-3-(2-propenyloxy)-

Base Information

• Chemical Name: 2-Propanol, 1-(phenylmethoxy)-3-(2-propenyloxy)-
• CAS No.: 83016-75-5
• Molecular Formula: C13H18O3
• Molecular Weight: 222.28000
• DSSTox Substance ID: DTXSID40444383
• Nikkaji Number: J1.497.363J
• Mol file: 83016-75-5.mol

Synonyms:83016-75-5;1-phenylmethoxy-3-prop-2-enoxypropan-2-ol;2-Propanol, 1-(phenylmethoxy)-3-(2-propenyloxy)-;1-(Phenylmethoxy)-3-(2-propen-1-yloxy)-2-propanol;1-(Allyloxy)-3-(benzyloxy)propan-2-ol;starbld0000939;SCHEMBL18653600;DTXSID40444383;AKOS030255315;1-(Allyloxy)-3-(benzyloxy)-2-propanol;FT-0673797

Chemical Property of 2-Propanol, 1-(phenylmethoxy)-3-(2-propenyloxy)-

Chemical Property:

• PSA: 38.69000
• LogP: 1.76670
• Solubility.: Dichloromethane
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 222.125594432
• Heavy Atom Count: 16
• Complexity: 176

Purity/Quality:

98% ^*data from raw suppliers

1-(Phenylmethoxy)-3-(2-propen-1-yloxy)-2-propanol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CCOCC(COCC1=CC=CC=C1)O
• Uses: 1-(Phenylmethoxy)-3-(2-propen-1-yloxy)-2-propanol (cas# 83016-75-5) is a compound useful in organic synthesis.

Technology Process of 2-Propanol, 1-(phenylmethoxy)-3-(2-propenyloxy)-

There total 4 articles about 2-Propanol, 1-(phenylmethoxy)-3-(2-propenyloxy)- 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%

3-allyloxy-1,2-propanediol (123-34-2) + benzyl bromide (100-39-0) → 1-O-benzyl-3-O-allyl-1,2,3-propanetriol (83016-75-5)

Guidance literature:

With tris(2,6-dimethylheptane-3,5-dionato)iron(III); potassium carbonate; In acetonitrile; at 80 ℃; regioselective reaction;

DOI:10.1002/chem.201504477

Reference yield: 93.0%

Benzyloxymethyl-oxiran (2930-05-4) + allyl alcohol (107-18-6) → 1-O-benzyl-3-O-allyl-1,2,3-propanetriol (83016-75-5)

Guidance literature:

With tris(pentafluorophenyl)borate; In dichloromethane; at 20 ℃; for 4h;

DOI:10.1016/S0040-4039(02)00703-7

Reference yield: 88.0%

Allyl glycidyl ether (106-92-3,25639-25-2,90907-93-0) + benzyl alcohol (100-51-6,185532-71-2) → 1-O-benzyl-3-O-allyl-1,2,3-propanetriol (83016-75-5)

Guidance literature:

With sodium hydride; at 20 ℃; for 4h;

DOI:10.1002/1099-0690(200103)2001:5<875::AID-EJOC875>3.0.CO;2-R

upstream raw materials:

3-allyloxy-1,2-propanediol

benzyl bromide

Allyl glycidyl ether

benzyl alcohol

Downstream raw materials:

6-benzyloxymethyl-2-iodomethyl-1,4-dioxane

2-benzyloxymethyl-6-hydroxymethyl-1,4-dioxane

2-acetoxymethyl-6-benzyloxymethyl-1,4-dioxane

6-benzyloxymethyl-2-p-nitrobenzoyloxymethyl-1,4-dioxane

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