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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678299Generated: October 31, 2026

Methanol → HCID 58912942, compound

https://huagongshe.com/reaction/1678299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
Reactant2-[4-(4-Hydroxyphenyl)butyl]-1H-isoindole-1,3(2H)-dioneHCID 22054451—
SolventDimethylformamideHCID 6228—
ProductHCID 58912942HCID 5891294259.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of sodium hydride in mineral oil (0.44 g of 60%) in anhydrous DMF (10 mL) was cooled to 0° C. N-[4-(4-hydroxyphenyl)butyl]phthalimide (2.95 g, 10 mmol) dissolved in dry DMF (15 ml) was added into the mixture which was then stirred for 30 min at 0° C. and allowed to warm to room temperature over 1 h. To the mixture was added portionwise N,N-dimethylthiocarbamoyl chloride (1.35 g, 11 mmol) dissolved in DMF (10 ml). The newly formed mixture was stirred at room temperature overnight, then at 50° C. for 1 h, and was cooled back to room temperature, at which point methanol (10 mL) was added into the mixture. The solvent was removed under reduced pressure. The residue was purified by flash chromatography over silica gel (dichloromethane/hexane/ethyl acetate, 10:1:0.2, v/v) to give N-{4-[4-(dimethythiocarbamoyloxy)phenyl]butyl}phthalimide 34 (2.27 g, 59%) as a slightly yellow solid. 1H NMR (300 MHz, CDCl3) δ 1.72 (m, 4H), 2.66 (m, 2H), 3.33 (s, 3H), 3.45 (s, 3H), 3.70 (m, 2H), 6.96 (d, 2H), 7.18 (d, 2H), 7.71 (m, 2H), 7.84 (m, 2H). m/z (ESI) 383 [C21H22N2O3S+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008494B2
Source datasetuspto-grants-2011_08
ORD IDord-d916f4e486e84e5cae60df075ccb24d7
Source noteuspto-grants-2011_08