Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258555Generated: November 2, 2026

Benzyl Bromide → HCID 10637344, compound

https://huagongshe.com/reaction/2258555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10821959HCID 10821959—
SolventDimethylformamideHCID 6228—
ProductHCID 10637344HCID 1063734490.7%

Reaction Steps

2-Chloro-3,4-dimethyl-6-nitrophenol (6.44 g, 31.9 mmol) was dissolved in dry DMF (105 mL) and flushed with argon. Benzyl bromide (4.17 mL,35.1 mmol) and K2CO3 (13.24 g, 95.7 mmol) were added. The reaction mixture was stirred at room temperature for 8 h (protected from light) and filtered. Water (5 mL) was added and the solvent was co-evaporated with xylene (2×150 mL) and CH2Cl2 (100 mL). The residue was mixed with CHCl3 (100 mL), filtered and after evaporation of the solvent 10.8 g of crude product remained. Purification by flash column chromatography (SiO2, CHCl3 -Hexane 1:1) gave the title compound (8.44 g). Mp: 74°-75° C.; 1H NMR (DMSO-d6): δ 7.80 (s, 1 H), 7.48-7.37 (m, 5 H), 5.06 (s, 2 H), 2.37 (s, 3 H), 2.34 (s, 3 H); 13C NMR (DMSO-d6): δ 145.24, 142.22, 142.08, 135.73, 134.73, 129.61, 128.39, 128.37, 128.35, 123.64, 75.74, 19.74, 17.13; MS (EI, 70 eV): m/z (rel.int.) 293/291 (M+, 0.08/0.37), 187/185 (8/24), 91 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05661183
Source datasetuspto-grants-1997_08
ORD IDord-2af1205037d94a1f8df06517e3410e84
Source noteuspto-grants-1997_08