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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487876Generated: October 30, 2026

Methyl iodide → Ethyl 2-(3-methoxyphenyl)-2-methylbutyrate

https://huagongshe.com/reaction/487876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl 2-methyl-2-[3-(1-methyl-2-oxo-1,2-dihydroquinolin-6-ylmethoxy)phenyl]butyrateHCID 67826098—
ProductEthyl 2-(3-methoxyphenyl)-2-methylbutyrateHCID 19091444—

Reaction Steps

The ethyl 2-(3-hydroxyphenyl)-2-methylbutyrate used as a starting material was obtained using the procedures described in the portion of Example 1 which is concerned with the preparation of starting materials except that methyl iodide was used in place of ethyl iodide in the second alkylation step. The intermediate so obtained, ethyl 2-(3-methoxyphenyl)-2-methylbutyrate, gave the following characteristic NMR signals: 0.84 (t, 3 H), 1.19 (t, 3 H), 1.5 (s, 3 H), 1.85-2.15 (m, 2 H), 3.8 (s, 3 H), 4.13 (q, 2 H), 6.72-6.92 (m, 3 H), 7.21 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298511
Source datasetuspto-grants-1994_03
ORD IDord-afd5e543d9fe4c899d316c2b215c1ad4
Source noteuspto-grants-1994_03