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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53254Generated: October 25, 2026

Methyl N-methylanthranilate → Methyl 2-(N-bromoacetyl-N-methylamino)benzoate

https://huagongshe.com/reaction/53254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl N-methylanthranilateHCID 6826—
ReactantSodium HydroxideHCID 14798—
ReactantBromoacetyl bromideHCID 61147—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(N-bromoacetyl-N-methylamino)benzoateHCID 1008536187.6%

Reaction Steps

A solution of bromoacetyl bromide (209 g) in dichloromethane (200 ml) was added dropwise to a cooled (ice bath) solution of methyl N-methylanthranilate (168 g) in dichloromethane (1.41). A solution of sodium hydroxide (59 g) in water (400 ml) was added dropwise and the reaction mixture was stirred at room temperature for 20 h. The organic phase was separated and washed with 1M hydrochloric acid (500 ml), brine (300 ml), saturated sodium hydrogen carbonate solution (400 ml), dried (Na2SO4) then evaporated to afford the required product (255 g). 1H NMR (360 MHz, CDCl3) δ3.23 (3H, s), 3.54 (1H, d, J=11 Hz), 3.60 (1H, d, J=11 Hz), 3.90 (3H, s), 7.40 (1H, d, J=8 Hz), 7.51 (1H, dd, J1 =J2 =8 Hz), 7.65 (1H, dd, J1 =J2 =8 Hz), 8.04 (1H, d, J=8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618812
Source datasetuspto-grants-1997_04
ORD IDord-3b0d53543bb343039b0c23b683e56ba3
Source noteuspto-grants-1997_04