(S)-2-(Dibenzylamino)butan-1-ol

Base Information

Chemical Name:(S)-2-(Dibenzylamino)butan-1-ol
CAS No.:249922-60-9
Molecular Formula:C18H23NO
Molecular Weight:269.387
Hs Code.:
DSSTox Substance ID:DTXSID801271523
Nikkaji Number:J964.052E
Mol file:249922-60-9.mol

Synonyms:(S)-2-(Dibenzylamino)butan-1-ol;249922-60-9;(2S)-2-(dibenzylamino)butan-1-ol;SCHEMBL3300438;RWDGCGHIPSWDTF-SFHVURJKSA-N;DTXSID801271523;(S)-2-(Dibenzylamino)-1-butanol;(S)-2-(dibenzylamino) butan-1-ol;AKOS037645425;AS-60710;(2S)-2-[Bis(phenylmethyl)amino]-1-butanol

Suppliers and Price of (S)-2-(Dibenzylamino)butan-1-ol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of (S)-2-(Dibenzylamino)butan-1-ol

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:269.177964357
Heavy Atom Count:20
Complexity:224

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(CO)N(CC1=CC=CC=C1)CC2=CC=CC=C2
Isomeric SMILES:CC[C@@H](CO)N(CC1=CC=CC=C1)CC2=CC=CC=C2

Technology Process of (S)-2-(Dibenzylamino)butan-1-ol

There total 3 articles about (S)-2-(Dibenzylamino)butan-1-ol 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: 97.3%

: 5856-62-2
(S)-2-aminobutan-1-ol

: 100-39-0
benzyl bromide

: 249922-60-9
(2S)-N,N-dibenzyl-2-aminobutan-1-ol

Guidance literature:: (S)-2-aminobutan-1-ol; With sodium hydroxide; potassium carbonate; In methanol; for 0.5h; Heating;

benzyl bromide; In methanol; for 6h; Heating;
DOI:10.1055/s-1999-3575

Reference yield:

: 205748-23-8
(R)-O-(2-bisphenylmethylamino)butyrylpantolactone

: 249922-60-9
(2S)-N,N-dibenzyl-2-aminobutan-1-ol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 16.5h;
DOI:10.1021/jo9712714

Reference yield:

: 103-49-1
dibenzylamine

: 249922-60-9
(2S)-N,N-dibenzyl-2-aminobutan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: tetra-n-butylammonium iodide; triethylamine / tetrahydrofuran / 20 °C

2: LiAlH₄ / tetrahydrofuran / 16.5 h / 20 °C

With lithium aluminium tetrahydride; tetra-(n-butyl)ammonium iodide; triethylamine; In tetrahydrofuran; 1: Substitution / 2: Reduction;
DOI:10.1021/jo9712714