C₁₅H₁₇IO₅

Base Information

Chemical Name:C₁₅H₁₇IO₅
CAS No.:1337981-87-9
Molecular Formula:C₁₅H₁₇IO₅
Molecular Weight:404.201
Hs Code.:

C<sub>15</sub>H<sub>17</sub>IO<sub>5</sub>

Synonyms:C₁₅H₁₇IO₅

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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 C₁₅H₁₇IO₅

Chemical Property:

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Technology Process of C₁₅H₁₇IO₅

There total 5 articles about C₁₅H₁₇IO₅ 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:

: 1337981-85-7
C₁₅H₁₉IO₅

: 1337981-87-9
C₁₅H₁₇IO₅

Guidance literature:: With sodium hypochlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutylammomium bromide; dihydrogen peroxide; sodium hydrogencarbonate; potassium bromide; In dichloromethane; at -10 - 20 ℃; Product distribution / selectivity;

Reference yield:

: 197899-19-7
(2R)-1-chloro-2-hydroxy-4-pentene

: 1337981-87-9
C₁₅H₁₇IO₅

Guidance literature:: Multi-step reaction with 5 steps

1: sodium cyanide / water / 30 - 45 °C

2: sulfuric acid / 20 °C

3: 1H-imidazole / dichloromethane; ethyl acetate / 25 - 30 °C

4: N-iodo-succinimide / acetone / 0 - 25 °C

5: sodium hydrogencarbonate; sodium hypochlorite; tetrabutylammomium bromide; dihydrogen peroxide; potassium bromide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / -10 - 20 °C

With 1H-imidazole; sodium cyanide; sodium hypochlorite; N-iodo-succinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sulfuric acid; tetrabutylammomium bromide; dihydrogen peroxide; sodium hydrogencarbonate; potassium bromide; In dichloromethane; water; ethyl acetate; acetone;

Reference yield:

: 181272-46-8
(2R)-1-cyano-2-hydroxy-4-pentene

: 1337981-87-9
C₁₅H₁₇IO₅

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid / 20 °C

2: 1H-imidazole / dichloromethane; ethyl acetate / 25 - 30 °C

3: N-iodo-succinimide / acetone / 0 - 25 °C

4: sodium hydrogencarbonate; sodium hypochlorite; tetrabutylammomium bromide; dihydrogen peroxide; potassium bromide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / -10 - 20 °C

With 1H-imidazole; sodium hypochlorite; N-iodo-succinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sulfuric acid; tetrabutylammomium bromide; dihydrogen peroxide; sodium hydrogencarbonate; potassium bromide; In dichloromethane; ethyl acetate; acetone;