1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol

Base Information

Chemical Name:1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol
CAS No.:67592-67-0
Molecular Formula:C₁₂H₁₆O₂Se
Molecular Weight:271.218
Hs Code.:

Synonyms:1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol

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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 1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol

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Technology Process of 1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol

There total 4 articles about 1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-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: 96.0%

: 106-92-3,25639-25-2,90907-93-0
Allyl glycidyl ether

: 1666-13-3
diphenyl diselenide

: 79092-14-1
2-hydroxy-1-phenylethyl phenyl selenide

: 67592-67-0
1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol

Guidance literature:: With sodium tetrahydroborate; In ethanol; Yields of byproduct given;
DOI:10.1021/jo961578n

Reference yield: 95.0%

: 106-92-3,25639-25-2,90907-93-0
Allyl glycidyl ether

: 1666-13-3
diphenyl diselenide

: 67592-67-0
1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol

Guidance literature:: With rongalite; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.333333h; regioselective reaction;
DOI:10.1055/s-0029-1216960

Reference yield: 93.0%

: 106-92-3,25639-25-2,90907-93-0
Allyl glycidyl ether

: 98-80-6
phenylboronic acid

: 67592-67-0
1-(prop-2'-eneoxy)-3-(selenophenyl)propan-2-ol

Guidance literature:: phenylboronic acid; With selenium; silver nitrate; In dimethyl sulfoxide; at 120 ℃; for 2h;

Allyl glycidyl ether; With potassium tert-butylate; In dimethyl sulfoxide; at 120 ℃; for 2h; stereoselective reaction;
DOI:10.1002/adsc.201800896