3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole

Base Information

Chemical Name:3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole
CAS No.:87671-63-4
Molecular Formula:C₂₅H₃₀NO₂P
Molecular Weight:407.492
Hs Code.:

Synonyms:3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole

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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 3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole

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Technology Process of 3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole

There total 3 articles about 3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole 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: 38.0%

: 63507-05-1
2,2-dimethyl-1-propyl diphenylphosphinite

: 614-70-0
2-ethylaminophenol

: 87671-63-4
3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole

Guidance literature:: With chloro-diisopropyl-amine; In diethyl ether; at -20 ℃;

Reference yield:

: 75-84-3
2,2-dimethyl-propanol-1

: 87671-63-4
3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / triethylamine / diethyl ether

2: 38 percent / N-chlorodi-isopropylamine / diethyl ether / -20 °C

With chloro-diisopropyl-amine; triethylamine; In diethyl ether;

Reference yield:

: 1079-66-9,74391-44-9
chloro-diphenylphosphine

: 87671-63-4
3-ethyl-2,3-dihydro-2-neopentoxy-2,2-diphenyl-1,3,2-benzoxazaphosph(V)ole

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / triethylamine / diethyl ether

2: 38 percent / N-chlorodi-isopropylamine / diethyl ether / -20 °C

With chloro-diisopropyl-amine; triethylamine; In diethyl ether;