Ethyl [4-(1-hydroxyethyl)phenyl]acetate

Base Information

Chemical Name:Ethyl [4-(1-hydroxyethyl)phenyl]acetate
CAS No.:58262-39-8
Molecular Formula:C12H16O3
Molecular Weight:208.25400
Hs Code.:
DSSTox Substance ID:DTXSID20597947

Synonyms:58262-39-8;Ethyl [4-(1-hydroxyethyl)phenyl]acetate;SCHEMBL1124844;DTXSID20597947;PQWVOQDOGCLIJP-UHFFFAOYSA-N;ethyl 4-(1-hydroxyethyl)phenylacetate;Ethyl 2-(4-(1-hydroxyethyl)phenyl)acetate;[4-(1-Hydroxy-ethyl)-phenyl]-acetic acid ethyl ester

Suppliers and Price of Ethyl [4-(1-hydroxyethyl)phenyl]acetate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Ethyl [4-(1-hydroxyethyl)phenyl]acetate

Chemical Property:

PSA：46.53000
LogP:1.84550
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:208.109944368
Heavy Atom Count:15
Complexity:195

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)CC1=CC=C(C=C1)C(C)O

Technology Process of Ethyl [4-(1-hydroxyethyl)phenyl]acetate

There total 2 articles about Ethyl [4-(1-hydroxyethyl)phenyl]acetate 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: 88.0%

: 1528-42-3
ethyl 4-acetylphenylacetate

: 58262-39-8
ethyl (4-(1-hydroxy)ethylphenyl)acetate

Guidance literature:: With sodium tetrahydroborate; In methanol; at 25 ℃; for 1h;
DOI:10.1016/j.bmc.2006.07.047

Reference yield:

: 101-97-3
Ethyl 2-phenylethanoate

: 58262-39-8
ethyl (4-(1-hydroxy)ethylphenyl)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 32 percent / AlCl₃ / CS₂ / Heating

2: 88 percent / sodium borohydride / methanol / 1 h / 25 °C

With sodium tetrahydroborate; aluminium trichloride; In methanol; carbon disulfide; 1: Friedel-Crafts reaction;
DOI:10.1016/j.bmc.2006.07.047