4-benzyloxytryptamine hydrochloride

Base Information

Chemical Name:4-benzyloxytryptamine hydrochloride
CAS No.:83788-94-7
Molecular Formula:C₁₇H₁₈N₂O*ClH
Molecular Weight:302.804
Hs Code.:

Synonyms:4-benzyloxytryptamine hydrochloride

Suppliers and Price of 4-benzyloxytryptamine hydrochloride

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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 4-benzyloxytryptamine hydrochloride

Chemical Property:

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Technology Process of 4-benzyloxytryptamine hydrochloride

There total 4 articles about 4-benzyloxytryptamine hydrochloride 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: 74.0%

: 83788-93-6
E-3-(2-nitrovinyl)-4-benzyloxyindole

: 83788-94-7
4-benzyloxytryptamine hydrochloride

Guidance literature:: With hydrogenchloride; lithium aluminium tetrahydride; In tetrahydrofuran; for 0.25h; Heating;
DOI:10.1002/jhet.5570190428

Reference yield:

: 20876-37-3
2-benzyloxy-6-nitrotoluene

: 83788-94-7
4-benzyloxytryptamine hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) pyrrolidine; 2.) 85percent N₂H₄ / 2.) Raney Ni / 1.) DMF, 125 deg C, 3 h; 2.) methanol, 50-60 deg C, 3 h

2: 76 percent / trifluoroacetic acid / 0.5 h / Ambient temperature

3: 74 percent / 1.) LiAlH₄; 2.) HCl / tetrahydrofuran / 0.25 h / Heating

With pyrrolidine; hydrogenchloride; lithium aluminium tetrahydride; hydrazine hydrate; nickel; In tetrahydrofuran; trifluoroacetic acid;
DOI:10.1002/jhet.5570190428

Reference yield:

: 20289-26-3
4-benzyloxy-1H-indole

: 83788-94-7
4-benzyloxytryptamine hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / trifluoroacetic acid / 0.5 h / Ambient temperature

2: 74 percent / 1.) LiAlH₄; 2.) HCl / tetrahydrofuran / 0.25 h / Heating

With hydrogenchloride; lithium aluminium tetrahydride; In tetrahydrofuran; trifluoroacetic acid;
DOI:10.1002/jhet.5570190428