(S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate

Base Information

Chemical Name:(S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate
CAS No.:885321-47-1
Molecular Formula:C₂₆H₃₅NO₆
Molecular Weight:457.567
Hs Code.:

Synonyms:(S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate

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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 (S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate

Chemical Property:

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Technology Process of (S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate

There total 4 articles about (S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate 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: 89.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 170937-77-6
(S)-2-tert-butoxycarbonylamino-1,1-diphenylpropane-1,3-diol

: 885321-47-1
(S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate

Guidance literature:: With sodium hydroxide; tetra-(n-butyl)ammonium iodide; In toluene; at 0 - 5 ℃; for 3h;
DOI:10.1016/j.tetasy.2005.12.027

Reference yield:

: 95715-86-9,108149-60-6
(S)-2,2-dimethyl-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-methyl ester

: 885321-47-1
(S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / diethyl ether / 3 h / 20 °C

2: 91 percent / aq. AcOH / 24 h / 20 °C

3: 89 percent / aq. NaOH; TBAI / toluene / 3 h / 0 - 5 °C

With sodium hydroxide; tetra-(n-butyl)ammonium iodide; acetic acid; In diethyl ether; toluene;
DOI:10.1016/j.tetasy.2005.12.027

Reference yield:

: phenylmagnesium bromide

: 885321-47-1
(S)-tert-butyl 2-(2-(tert-butoxycarbonylamino)-3-hydroxy-3,3-diphenylpropoxy)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / diethyl ether / 3 h / 20 °C

2: 91 percent / aq. AcOH / 24 h / 20 °C

3: 89 percent / aq. NaOH; TBAI / toluene / 3 h / 0 - 5 °C

With sodium hydroxide; tetra-(n-butyl)ammonium iodide; acetic acid; In diethyl ether; toluene;
DOI:10.1016/j.tetasy.2005.12.027