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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487878Generated: October 31, 2026

Allyl bromide → Ethyl 2-allyl-2-(3-methoxyphenyl)butyrate

https://huagongshe.com/reaction/487878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl 2-allyl-2-[3-(1-methyl-2-oxo-1,2-dihydroquinolin-6-ylmethoxy)phenyl]butyrateHCID 57452573—
ProductEthyl 2-allyl-2-(3-methoxyphenyl)butyrateHCID 19091449—

Reaction Steps

The ethyl 2-allyl-2-(3-hydroxyphenyl)butyrate 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 allyl bromide was used in place of ethyl iodide in the second alkylation step. The intermediate so obtained, ethyl 2-allyl-2-(3-methoxyphenyl)butyrate gave the following characteristic NMR signals: 0.76 (t, 3 H), 1.18 (t, 3 H), 2.05 (m, 2 H), 2.75 (m, 2 H), 3.80 (s, 3 H), 4.15 (q, 2 H), 5.15 (m, 2 H), 5.50 (m, 1 H), 6.80 (m, 3 H), 7.22 (m, 1 H). ##STR2##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298511
Source datasetuspto-grants-1994_03
ORD IDord-ddf3ee14de3944b1bfa61c1c8354cf89
Source noteuspto-grants-1994_03