C₃₄H₃₃O₅P

Base Information

Chemical Name:C₃₄H₃₃O₅P
CAS No.:1233333-87-3
Molecular Formula:C₃₄H₃₃O₅P
Molecular Weight:552.607
Hs Code.:

C<sub>34</sub>H<sub>33</sub>O<sub>5</sub>P

Synonyms:C₃₄H₃₃O₅P

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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 C₃₄H₃₃O₅P

Chemical Property:

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Technology Process of C₃₄H₃₃O₅P

There total 6 articles about C₃₄H₃₃O₅P 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:

: 1337981-67-5
C₁₆H₁₉BrO₅

: 603-35-0
triphenylphosphine

: 1233333-87-3
C₃₄H₃₃O₅P

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at -10 - 20 ℃;

Reference yield:

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

: 1233333-87-3
C₃₄H₃₃O₅P

Guidance literature:: Multi-step reaction with 6 steps

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

2: hydrogenchloride / 20 °C

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

4: N-Bromosuccinimide / acetone / 0 - 40 °C

5: sodium hydrogencarbonate; sodium hypochlorite; N-benzyl-N,N,N-triethylammonium chloride; potassium bromide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / hexane / -10 - 20 °C

6: potassium carbonate / N,N-dimethyl-formamide / -10 - 20 °C

With 1H-imidazole; hydrogenchloride; sodium cyanide; sodium hypochlorite; N-Bromosuccinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; N-benzyl-N,N,N-triethylammonium chloride; sodium hydrogencarbonate; potassium carbonate; potassium bromide; In hexane; dichloromethane; water; N,N-dimethyl-formamide; acetone; 6: Wittig Reaction;

Reference yield:

: 1233333-89-5
C₁₆H₂₀O₄

: 1233333-87-3
C₃₄H₃₃O₅P

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide / acetone / 0 - 40 °C

2: sodium hydrogencarbonate; sodium hypochlorite; N-benzyl-N,N,N-triethylammonium chloride; potassium bromide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / hexane / -10 - 20 °C

3: potassium carbonate / N,N-dimethyl-formamide / -10 - 20 °C

With sodium hypochlorite; N-Bromosuccinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; N-benzyl-N,N,N-triethylammonium chloride; sodium hydrogencarbonate; potassium carbonate; potassium bromide; In hexane; N,N-dimethyl-formamide; acetone; 3: Wittig Reaction;