(+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester

Base Information

Chemical Name:(+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester
CAS No.:127152-71-0
Molecular Formula:C₃₄H₃₃N₅O₂
Molecular Weight:543.668
Hs Code.:

Synonyms:(+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester

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Chemical Property of (+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester

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Technology Process of (+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester

There total 3 articles about (+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester 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: 59.0%

: 81477-91-0
benzyl 2-(diphenylmethyleneamino)acetate

: 127152-62-9
5-<4-(bromomethyl)phenyl>-2-(1,1-dimethylethyl)-2H-tetrazole

: 127152-71-0
(+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester

Guidance literature:: With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; for 5h; Ambient temperature;
DOI:10.1021/jm00107a037

Reference yield:

: 127152-61-8
5-(4-methylphenyl)-2-(1,1-dimethylethyl)-2H-tetrazole

: 127152-71-0
(+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: N-bromosuccinimide (NBS), benzoyl peroxide / CCl₄ / Heating

2: 59 percent / 10percent aq. NaOH / tetrabutyl ammonium sulfate / CH₂Cl₂ / 5 h / Ambient temperature

With sodium hydroxide; N-Bromosuccinimide; Perbenzoic acid; tetra(n-butyl)ammonium hydrogensulfate; In tetrachloromethane; dichloromethane;
DOI:10.1021/jm00107a037

Reference yield:

: 24994-04-5
5-(4-methylphenyl)-2H-tetrazole

: 127152-71-0
(+/-)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>-α-<(diphenylmethylene)amino>benzenepropanoic acid phenylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 65 percent / conc. H₂SO₄ / trifluoroacetic acid / 3 h / Ambient temperature

2: N-bromosuccinimide (NBS), benzoyl peroxide / CCl₄ / Heating

3: 59 percent / 10percent aq. NaOH / tetrabutyl ammonium sulfate / CH₂Cl₂ / 5 h / Ambient temperature

With sodium hydroxide; N-Bromosuccinimide; Perbenzoic acid; sulfuric acid; tetra(n-butyl)ammonium hydrogensulfate; In tetrachloromethane; dichloromethane; trifluoroacetic acid;
DOI:10.1021/jm00107a037