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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435143Generated: October 25, 2026

N-bromobutanimide → Methyl 4-(bromomethyl)-3-nitrobenzoate

https://huagongshe.com/reaction/435143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 4-methyl-3-nitrobenzoateHCID 81816—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 4-(bromomethyl)-3-nitrobenzoateHCID 13399987—

Reaction Steps

All of the 4-methoxycarbonyl-2-nitrotoluene obtained as described above was dissolved in carbon tetrachloride. Approximately 14.2 g (0.082 mole) of N-bromosuccinimide was added to the carbon tetrachloride solution. The resulting solution was heated to reflux temperature and stirred for approximately 64 hours. The solution was cooled and the succinimide was removed by vacuum filtration. The remaining solution was concentrated on a rotary evaporator using water aspirator vacuum. The synthesis produced 24 g of 4-methoxycarbonyl-2-nitrobenzyl bromide. The cholate ester of this product was then prepared as described for the preparation of the esters in Section B. The O,O,O-triacetyl derivative was also prepared as described in Section F.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400461
Source datasetuspto-grants-1983_08
ORD IDord-2098fbb8c47a4459a83564039f42c795
Source noteuspto-grants-1983_08