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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377197Generated: October 31, 2026

Benzyl Bromide → Methyl 4-benzyloxy-3-tert-butyl-5-iodobenzoate

https://huagongshe.com/reaction/2377197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-t-butyl-4-hydroxy-5-iodobenzoateHCID 12084815—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-benzyloxy-3-tert-butyl-5-iodobenzoateHCID 1208481680%

Reaction Steps

24.1 g (72 mmol) of methyl 3-tert-butyl-4-hydroxy-5-iodobenzoate are dissolved in 200 mL of dimethylformamide. 3.47 g (86 mmol) of 60% sodium hydride are added slowly and the reaction medium is stirred for 1 hour. 9.4 mL (79 mmol) of benzyl bromide are then added and the medium is stirred at room temperature for 2 hours, and is then hydrolysed and extracted with ethyl ether. The organic phase is washed 3 times with water and then concentrated under reduced pressure. The residue is purified by chromatography (eluent: 98 heptane/2 ethyl acetate). A yellow oil is obtained (m=24.3 g; yield=80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468457B2
Source datasetuspto-grants-2008_12
ORD IDord-b74b099914ac49539d1ba15387f66d1b
Source noteuspto-grants-2008_12