(2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

Base Information

Chemical Name:(2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine
CAS No.:1028547-07-0
Molecular Formula:C₂₄H₃₀INO₅
Molecular Weight:539.41
Hs Code.:

Synonyms:(2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

Suppliers and Price of (2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

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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 (2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

Chemical Property:

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Technology Process of (2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

There total 11 articles about (2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine 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: 49.0%

: 1045858-93-2
(2S,3R)-2-[(4-bromophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

: 1028547-07-0
(2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

Guidance literature:: With copper(l) iodide; Trimethylenediamine; sodium iodide; at 120 ℃;
DOI:10.1002/jlcr.1242

Reference yield:

: 24393-53-1,136265-11-7,15795-20-7
ethyl (E)-3-(4-bromophenyl)-2-propenoate

: 1028547-07-0
(2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

Guidance literature:: Multi-step reaction with 10 steps

1: 72 percent / DIBAL-H

2: 74 percent / t-BuOOH; (+)-DIPT / Ti(O-iPr)4

3: 65 percent / NEt₃; DMAP

4: 49 percent / ammonium hydroxide

5: 83 percent / NEt₃

6: 79 percent / tBuO(-)*Na(+)

7: 62 percent / borane-THF

8: 75 percent / NEt₃; DMAP

9: 49 percent / NaI; CuI; NH₂(CH₂)3NH₂ / 120 °C

With tert.-butylhydroperoxide; dmap; ammonium hydroxide; copper(l) iodide; borane-THF; L-(+)-diisopropyl tartrate; diisobutylaluminium hydride; Trimethylenediamine; triethylamine; sodium iodide; titanium(IV) isopropylate; 2: Sharpless asymmetric epoxidation;
DOI:10.1002/jlcr.1242

Reference yield:

: 105515-33-1
(2E)-3-(4-bromophenyl)prop-2-en-1-ol

: 1028547-07-0
(2S,3R)-2-[(4-iodophenyl)-(2-ethoxyphenoxy)methyl]-N-tert-butoxycarbonylmorpholine

Guidance literature:: Multi-step reaction with 9 steps

1: 74 percent / t-BuOOH; (+)-DIPT / Ti(O-iPr)4

2: 65 percent / NEt₃; DMAP

3: 49 percent / ammonium hydroxide

4: 83 percent / NEt₃

5: 79 percent / tBuO(-)*Na(+)

6: 62 percent / borane-THF

7: 75 percent / NEt₃; DMAP

8: 49 percent / NaI; CuI; NH₂(CH₂)3NH₂ / 120 °C

With tert.-butylhydroperoxide; dmap; ammonium hydroxide; copper(l) iodide; borane-THF; L-(+)-diisopropyl tartrate; Trimethylenediamine; triethylamine; sodium iodide; titanium(IV) isopropylate; 1: Sharpless asymmetric epoxidation;
DOI:10.1002/jlcr.1242