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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908025Generated: October 27, 2026

Iodoethane → Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate

https://huagongshe.com/reaction/1908025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)(tert-butoxy)formamideHCID 801162—
CatalystBenzyltriethylammonium bromideHCID 165294—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductTert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamateHCID 5818056271.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

tert-Butyl N-(1,3-dioxoisoindolin-2-yl)carbamate (1.0 g, 3.8 mmol), iodoethane (460 μL, 5.7 mmol), potassium carbonate (2.1 g, 15 mmol), and benzyl-triethyl-ammonium bromide (210 mg, 0.80 mmol) were combined in acetonitrile (15 mL) and heated at 50° C. for 48 h. The reaction mixture was diluted with water (30 mL) and was extracted with ether (3×15 mL). The combined organics were washed with brine, dried over sodium sulfate and evaporated to dryness. The crude material was purified by column chromatography (0-20% ethyl acetate in hexanes) to afford tert-butyl 1,3-dioxoisoindolin-2-yl(ethyl)-carbamate (0.79 g, 71%). ESI-MS m/z calc. 290.1. found 291.3 (M+1)+; Retention time: 1.64 minutes (3 min run). 1H NMR (400 MHz, CDCl3) δ 7.98-7.85 (m, 2H), 7.84-7.69 (m, 2H), 3.86-3.57 (m, 2H), 1.52 (s, 3H), 1.32 (s, 6H), 1.27-1.04 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-5a70391081e7493e9619ea537b5fc19c
Source noteuspto-grants-2013_12