(1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol

Base Information

Chemical Name:(1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol
CAS No.:1210046-66-4
Molecular Formula:C₁₆H₁₇ClO₃
Molecular Weight:292.762
Hs Code.:

Synonyms:(1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-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 (1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol

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Technology Process of (1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol

There total 2 articles about (1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-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: 94.0%

: 124014-00-2
5-(4-methoxy-5-chlorophenyl)furan-2-carbaldehyde

: 6737-11-7
2-acetoxy-3-butene

: 1210046-66-4
(1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol

Guidance literature:: With potassium phosphate; C₅₀H₃₉IrN₂O₆P₂; water; isopropyl alcohol; In tetrahydrofuran; at 70 ℃; for 48h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/jo902697g

Reference yield:

: 6737-11-7
2-acetoxy-3-butene

: 443289-30-3
[5-(3-chloro-4-methoxyphenyl)furan-2-yl]methanol

: 1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol

: 1210046-66-4
(1R,2R)-1-[5-(3-chloro-4-methoxyphenyl)furan-2-yl]-2-methylbut-3-en-1-ol

Guidance literature:: With potassium phosphate; C₅₀H₃₉IrN₂O₆P₂; water; In tetrahydrofuran; at 70 ℃; for 48h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/jo902697g