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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426304Generated: November 2, 2026

Dimethylamine → Methyl 3-bromo-5-((dimethylamino)methyl)benzoate

https://huagongshe.com/reaction/1426304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTetrahydrofuranHCID 8028—
Reactant1,3-Benzenedicarboxylic acid, 5-bromo-, 1,3-dimethyl esterHCID 103954—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 3-bromo-5-formylbenzoateHCID 11436457—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-bromo-5-((dimethylamino)methyl)benzoateHCID 5818796293%

Reaction Steps

To a solution of methyl 3-bromo-5-formylbenzoate (1.8 g, 7.4 mmol, prepared as described in WO2003/048111 starting from dimethyl 5-bromoisophthalate (Alfa Aesar) in methylene chloride (20 mL) was added a solution of 2.0M dimethylamine in tetrahydrofuran (7.4 mL, 15 mmol) and the reaction was stirred for 15 min. Sodium triacetoxyborohydride (4.7 g, 22 mmol) was then added and the resulting mixture was stirred overnight. Saturated sodium bicarbonate solution was added and the resulting mixture was extracted with ethyl acetate. The organic extract was washed twice with water, once with brine, dried over sodium sulfate, filtered and concentrated to afford product as a light yellow oil (1.87 g, 93%). 1H NMR (400 MHz, CDCl3) δ 8.08-8.03 (m, 1H), 7.90-7.87 (m, 1H), 7.70-7.67 (m, 1H), 3.91 (s, 3H), 3.42 (s, 2H), 2.24 (s, 6H); LCMS (M+H)+: 272.0, 274.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933085B2
Source datasetuspto-grants-2015_01
ORD IDord-b4c2871d2fe64dfab8422307547299cc
Source noteuspto-grants-2015_01