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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723170Generated: October 30, 2026

N-(4-Bromobutyl)phthalimide → N-(4-METHYLSULFANYL-BUTYL)PHTHALIMIDE

https://huagongshe.com/reaction/723170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Bromobutyl)phthalimideHCID 93575—
ReactantSodium methanethiolateHCID 4378561—
SolventMethanolHCID 887—
ProductN-(4-METHYLSULFANYL-BUTYL)PHTHALIMIDEHCID 1096413691%

Reaction Steps

A solution of 2-(4-bromo-butyl)-isoindole-1,3-dione (1.00 g, 3.54 mmol) in MeOH (60 mL) was treated with sodium thiomethoxide (0.298 g, 4.25 mmol) and heated to reflux 18 h. The solvent was evaporated in vacuo and the residue partitioned between EtOAc and water. The aqueous layer was further extracted with EtOAc (1×75 mL). The organic layers were dried over MgSO4 and concentrated in vacuo to afford the product 2-(4-methylsulfanyl-butyl)-isoindole-1,3-dione (0.803 g, 91%). 1H NMR (MeOD) 7.844 (m, 4H), 3.704 (t, 2H, J=7.2 Hz), 2.549 (t, 2H, J=7.2 Hz), 2.063 (s, 3H), 1.792 (quint, 2H, J=7.2 Hz), 1.731 (quint, 2H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138530B2
Source datasetuspto-grants-2006_11
ORD IDord-8fac5d27bd574830a23c8f29c19ef8f1
Source noteuspto-grants-2006_11