2-acetoxypropyl tosylate

Base Information

Chemical Name:2-acetoxypropyl tosylate
CAS No.:103745-04-6
Molecular Formula:C₁₂H₁₆O₅S
Molecular Weight:272.322
Hs Code.:

Synonyms:2-acetoxypropyl tosylate

Suppliers and Price of 2-acetoxypropyl tosylate

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

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Chemical Property of 2-acetoxypropyl tosylate

Chemical Property:

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Technology Process of 2-acetoxypropyl tosylate

There total 8 articles about 2-acetoxypropyl tosylate 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: 68.0%

: 32464-98-5,102044-99-5,103775-61-7,54619-31-7
toluene-4-sulfonic acid 2-hydroxypropyl ester

: 75-36-5
acetyl chloride

: 103745-04-6
2-acetoxypropyl tosylate

Guidance literature:: With triethylamine;

Reference yield: 48.0%

: 1192-62-7,80145-44-4
1-(2-furyl)-1-ethanone

: 57-55-6,63625-56-9
propylene glycol

: 104-15-4
toluene-4-sulfonic acid

: 26923-94-4
Propan-1,2-diol-acetat-tosylat

: 103745-04-6
2-acetoxypropyl tosylate

Guidance literature:: In benzene; Heating;
DOI:10.1016/S0040-4039(98)00185-3

Reference yield:

: 57-55-6,63625-56-9
propylene glycol

: 108-24-7
acetic anhydride

: 98-59-9
p-toluenesulfonyl chloride

: 103745-04-6
2-acetoxypropyl tosylate

Guidance literature:: propylene glycol; p-toluenesulfonyl chloride; With di(n-butyl)tin oxide; triethylamine; In dichloromethane; at 20 ℃; Inert atmosphere;

acetic anhydride; With pyridine; at 20 ℃; Inert atmosphere;

With Porcine Pancreas Lipase; In di-isopropyl ether; at 30 ℃; for 24h; pH=6.5; regioselective reaction; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1016/j.tetasy.2009.11.005