Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425634Generated: November 1, 2026

1,3-dimethyl 5-(2,5-dimethyl-1H-pyrrol-1-yl)benzene-1,3-dicarboxylate → HCID 59440796, compound

https://huagongshe.com/reaction/1425634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-dimethyl 5-(2,5-dimethyl-1H-pyrrol-1-yl)benzene-1,3-dicarboxylateHCID 722206—
ReactantDibahHCID 16682954—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59440796HCID 5944079697%

Reaction Steps

To a solution of 9 (2.87 g, 10 mmol) in THF (60 mL) at −78° C. was added Dibal-H (1 M solution in toluene, 60 mL, 60 mmol) drop wise. The reaction mixture was slowly warmed to room temperature over a period of 6 h, and then quenched by sodium potassium tartrate (1 M, 40 mL). The THF was removed by rotary evaporation, and the resulting aqueous solution was extracted by ether (3×100 mL). The combined organic layers were dried over Na2SO4 and concentrated. The crude product was purified by flash column chromatography (EtOAc/hexanes, 2:1-4:1) to yield 10 (2.24 g, 97%) as a white solid (Caution: the product is not stable as solution forms, while stable in solid form for weeks at room temperature): 1H NMR (500 MHz, CDCl3) δ 2.01 (s, 6H), 2.45 (s, 2H), 4.69-4.70 (d, J=5.5 Hz, 4H), 5.89 (s, 2H), 7.10 (s, 2H), 7.39 (s, 1H); 13C NMR (125 MHz, CDCl3) δ13.1, 64.5, 105.8, 124.3, 125.6, 128.7, 139.3, 142.4; LC-MS (M+H+) calcd for C14H18NO2 232, found 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08932842B2
Source datasetuspto-grants-2015_01
ORD IDord-00717ee938d34c49b6e4291105654a03
Source noteuspto-grants-2015_01