C₁₇H₂₄O₅

Base Information

Chemical Name:C₁₇H₂₄O₅
CAS No.:1294005-32-5
Molecular Formula:C₁₇H₂₄O₅
Molecular Weight:308.375
Hs Code.:

C<sub>17</sub>H<sub>24</sub>O<sub>5</sub>

Synonyms:C₁₇H₂₄O₅

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Chemical Property of C₁₇H₂₄O₅

Chemical Property:

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Technology Process of C₁₇H₂₄O₅

There total 5 articles about C₁₇H₂₄O₅ 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: 99.0%

: 77-76-9
2,2-dimethoxy-propane

: (2S,3R)-5-Benzyloxy-2,3-dihydroxy-pentanoic acid ethyl ester

: 1294005-32-5
C₁₇H₂₄O₅

Guidance literature:: With toluene-4-sulfonic acid; In acetone; at 20 ℃; for 12h;
DOI:10.1016/j.tetlet.2011.02.014

Reference yield:

: 19790-60-4
3-Benzyloxypropanal

: 1294005-32-5
C₁₇H₂₄O₅

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / tetrahydrofuran / 3 h / 0 - 20 °C

2: potassium osmate(VI) dihydrate; (DHQD)2PHAL; methanesulfonamide; K₃[Fe(CN)6]; potassium carbonate / water; tert-butyl alcohol / 24 h / 0 °C

3: toluene-4-sulfonic acid / acetone / 12 h / 20 °C

With potassium osmate(VI) dihydrate; (DHQD)2PHAL; methanesulfonamide; K₃[Fe(CN)6]; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; water; acetone; tert-butyl alcohol; 1: Horner-Wittig olefination;
DOI:10.1016/j.tetlet.2011.02.014

Reference yield:

: 100-39-0
benzyl bromide

: 1294005-32-5
C₁₇H₂₄O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 12 h / 0 - 20 °C

2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.17 h / -78 °C

2.2: 0.75 h

2.3: 1.5 h / -78 - 20 °C

3.1: sodium hydride / tetrahydrofuran / 3 h / 0 - 20 °C

4.1: potassium osmate(VI) dihydrate; (DHQD)2PHAL; methanesulfonamide; K₃[Fe(CN)6]; potassium carbonate / water; tert-butyl alcohol / 24 h / 0 °C

5.1: toluene-4-sulfonic acid / acetone / 12 h / 20 °C

With potassium osmate(VI) dihydrate; (DHQD)2PHAL; oxalyl dichloride; methanesulfonamide; K₃[Fe(CN)6]; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; dimethyl sulfoxide; In tetrahydrofuran; dichloromethane; water; acetone; tert-butyl alcohol; 2.1: Swern oxidation / 2.2: Swern oxidation / 2.3: Swern oxidation / 3.1: Horner-Wittig olefination;
DOI:10.1016/j.tetlet.2011.02.014