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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270324Generated: November 1, 2026

N-(4-Bromobutyl)phthalimide → HCID 18416782, compound

https://huagongshe.com/reaction/2270324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Bromobutyl)phthalimideHCID 93575—
Reactant2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
ReactantHCID 54072529HCID 54072529—
ProductHCID 18416782HCID 1841678288%

Reaction Steps

Following the procedure as outlined in Example 9, 6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-(4-methoxy-benzenesulfonyl)-2-methyl-hexanoic acid ethyl ester was prepared, starting from (5.0 g, 20 mmol) of 2-(4-methoxy-benzenesulfonyl)-acetic acid ethyl ester and 4-phathalimido bromobutane (5.66 g, 20 mmol). Yield 8.4 g, 97%; Colorless oil; MS: 474 (M+H). Starting from 6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-(4-methoxy-benzenesulfonyl)-2-methyl-hexanoic acid ethyl ester (8.4 g, 17.7 mmol) 6;95 g (88%) of 6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-2-(4-methoxy-benzenesulfonyl)-2-methyl-hexanoic acid was isolated as colorless oil by following the procedure as outlined in Example 9. MS: 446 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331563B1
Source datasetuspto-grants-2001_12
ORD IDord-e29271f6f0fb4368af6fec7b30154654
Source noteuspto-grants-2001_12