(3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester

Base Information

Chemical Name:(3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester
CAS No.:906457-92-9
Molecular Formula:C₂₀H₂₃BrO₅
Molecular Weight:423.304
Hs Code.:

(3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid <i>tert</i>-butyl ester

Synonyms:(3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester

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Chemical Property of (3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester

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Technology Process of (3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester

There total 4 articles about (3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl 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: 89.0%

: 906457-91-8
3-benzyloxy-2-bromo-5-hydroxymethyl-phenol

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

: 906457-92-9
(3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester

Guidance literature:: With potassium carbonate; sodium iodide; 18-crown-6 ether; In acetone; for 24h; Heating;
DOI:10.1021/ja0622406

Reference yield:

: 906457-90-7
3-benzyloxy-4-bromo-5-hydroxy-benzoic acid ethyl ester

: 906457-92-9
(3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / (CH₃)2S*BH₃ / tetrahydrofuran / 36 h / Heating

2: 89 percent / potassium carbonate; sodium iodide / 18-crown-6 / acetone / 24 h / Heating

With dimethylsulfide borane complex; potassium carbonate; sodium iodide; 18-crown-6 ether; In tetrahydrofuran; acetone;
DOI:10.1021/ja0622406

Reference yield:

: 100-39-0
benzyl bromide

: 906457-92-9
(3-benzyloxy-2-bromo-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 37 percent / potassium carbonate / 18-crown-6 / acetone / 8 h / Heating

2: 90 percent / (CH₃)2S*BH₃ / tetrahydrofuran / 36 h / Heating

3: 89 percent / potassium carbonate; sodium iodide / 18-crown-6 / acetone / 24 h / Heating

With dimethylsulfide borane complex; potassium carbonate; sodium iodide; 18-crown-6 ether; In tetrahydrofuran; acetone;
DOI:10.1021/ja0622406