(R)-hydroprene

Base Information

Chemical Name:(R)-hydroprene
CAS No.:65733-19-9
Molecular Formula:C₁₇H₃₀O₂
Molecular Weight:266.424
Hs Code.:
DSSTox Substance ID:DTXSID8058241
Wikidata:Q27119778
Metabolomics Workbench ID:56201

Synonyms:(R)-hydroprene;ethyl (2E,4E,7R)-3,7,11-trimethyldodeca-2,4-dienoate;SCHEMBL2231129;DTXSID8058241;CHEBI:39235;Q27119778;65733-19-9

Suppliers and Price of (R)-hydroprene

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (R)-hydroprene

Chemical Property:

XLogP3:6.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:10
Exact Mass:266.224580195
Heavy Atom Count:19
Complexity:300

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C
Isomeric SMILES:CCOC(=O)/C=C(\C)/C=C/C[C@H](C)CCCC(C)C

Technology Process of (R)-hydroprene

There total 22 articles about (R)-hydroprene 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: 92.0%

: (2E,4E)-3,7,11-trimethyl-2,4-dodecadienoic acid

: 1609-47-8
diethyl dicarbonate

: 36557-30-9,41096-46-2,41096-47-3,41205-09-8,53042-55-0,53042-72-1,53042-73-2,53833-71-9,57378-83-3,57378-84-4,65733-19-9,65733-18-8
(S)-hydroprene

Guidance literature:: With dmap; In toluene; at 15 - 25 ℃; for 2h; Reagent/catalyst; Solvent; Temperature; Green chemistry;

Reference yield: 79.0%

: 1356399-81-9
C₁₁H₂₃BO₂

: 122135-84-6,137273-43-9,122135-96-0
ethyl (E)-3-(trifluoromethylsulfonyloxy)but-2-enoate

: 36557-30-9,41096-46-2,41096-47-3,41205-09-8,53042-55-0,53042-72-1,53042-73-2,53833-71-9,57378-83-3,57378-84-4,65733-19-9,65733-18-8
(S)-hydroprene

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; In 1,4-dioxane; water; at 80 ℃; for 20h; Inert atmosphere;
DOI:10.1016/j.tetlet.2012.02.019

Reference yield:

: 106-22-9
Citronellol

: 36557-30-9,41096-46-2,41096-47-3,41205-09-8,53042-55-0,53042-72-1,53042-73-2,53833-71-9,57378-83-3,57378-84-4,65733-19-9,65733-18-8
(S)-hydroprene

Guidance literature:: Multi-step reaction with 5 steps

1: 93 percent / H₂ / Pd/C / methanol / 50 h / 20 °C

2: PCC / CH₂Cl₂ / 2 h / 20 °C

3: 82 percent / diethyl ether / 15 h / 20 °C

4: 1.) O₃, O₂, 2.) Me₂S, 3.) Na₂SO₄, TsOH*H₂O / 1.) CH₂Cl₂, MeOH, -65 deg C, 2.) -60 deg C, 1h; -15 deg C, 1 h; 0 deg C, 1 h; 20 deg C, 12 h, 3.) benzene, reflux, 1 h

5: 2.) 10percent H₂SO₄ / 1.) ether, -10 deg C, 3 h, 2.) 1h

With dimethylsulfide; sulfuric acid; hydrogen; oxygen; toluene-4-sulfonic acid; ozone; sodium sulfate; pyridinium chlorochromate; palladium on activated charcoal; In methanol; diethyl ether; dichloromethane;
DOI:10.1007/BF00699985