Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508807Generated: October 29, 2026

N-bromobutanimide → Methyl 4-(bromomethyl)-2-methoxybenzoate

https://huagongshe.com/reaction/508807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-methoxy-4-methylbenzoateHCID 7172021—
CatalystAzobisisobutyronitrileHCID 6547—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 4-(bromomethyl)-2-methoxybenzoateHCID 1128839870.2%

Reaction Steps

To a solution of methyl 2-methoxy-4-methylbenzoate (10.00 g, 55 mmol) in CCl4 (150 mL) were added NBS (11.8 g, 66 mmol) and AIBN (0.100 g). The reaction mixture was refluxed for 18 h. The reaction mass was diluted with diethyl ether and washed with 25% NaOH solution. The organic layer was dried over anhydrous sodium sulphate and concentrated to afford 10.00 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 3.77 (m, 6H), 4.68 (s, 2H), 7.06 (d, J=7.8 Hz, 1H), 7.23 (s, 1H), 7.61 (d, J=7.8 Hz, 1H); MS (m/z): 259.13 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096545B2
Source datasetuspto-grants-2015_08
ORD IDord-377ad810371d4520b20cbffeec254d8c
Source noteuspto-grants-2015_08