2(3H)-Furanone, dihydro-3-[(phenylmethoxy)methoxy]-, (S)-

Base Information

Chemical Name:2(3H)-Furanone, dihydro-3-[(phenylmethoxy)methoxy]-, (S)-
CAS No.:73991-96-5
Molecular Formula:C12H14O4
Molecular Weight:222.241
Hs Code.:
DSSTox Substance ID:DTXSID90455444
Wikidata:Q82277432

Synonyms:73991-96-5;2(3H)-Furanone, dihydro-3-[(phenylmethoxy)methoxy]-, (S)-;DTXSID90455444

Suppliers and Price of 2(3H)-Furanone, dihydro-3-[(phenylmethoxy)methoxy]-, (S)-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 2(3H)-Furanone, dihydro-3-[(phenylmethoxy)methoxy]-, (S)-

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:222.08920892
Heavy Atom Count:16
Complexity:223

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC(=O)C1OCOCC2=CC=CC=C2
Isomeric SMILES:C1COC(=O)[C@H]1OCOCC2=CC=CC=C2

Technology Process of 2(3H)-Furanone, dihydro-3-[(phenylmethoxy)methoxy]-, (S)-

There total 1 articles about 2(3H)-Furanone, dihydro-3-[(phenylmethoxy)methoxy]-, (S)- 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: 79.0%

: 3587-60-8
Benzyloxymethyl chloride

: 52079-23-9
(3S)-3-hydroxydihydrofuran-2(3H)-one

: 73991-96-5
(S)-3-hydroxybutyrolactone, benzyloxy methyl ether

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In 1,2-dimethoxyethane; at 65 ℃; for 2h;
DOI:10.1016/0040-4020(95)00037-9

Reference yield: 73.0%

: 73991-96-5
(S)-3-hydroxybutyrolactone, benzyloxy methyl ether

: 141806-46-4,141806-56-6
(3S)-2,3,4,5-tetrahydro-3-<(benzyloxy)methoxy>-2-hydroxyfuran

Guidance literature:: With diisobutylaluminium hydride; In diethyl ether; at -78 - 0 ℃; for 4h;
DOI:10.1016/0040-4020(95)00037-9

Reference yield:

: 73991-96-5
(S)-3-hydroxybutyrolactone, benzyloxy methyl ether

: 74888-88-3,74888-90-7
(3S,4S)-3-Benzyloxymethoxy-1-(tert-butyl-dimethyl-silanyloxy)-4,7-dimethyl-oct-7-en-4-ol

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / -78 °C

2: imidazole / dimethylformamide

3: tetrahydrofuran / -78 °C

With 1H-imidazole; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/ja00526a074