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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908086Generated: October 31, 2026

Methyl 3-bromo-4-(tert-butyl)benzoate → Methyl 4-tert-butyl-3-cyano-benzoate

https://huagongshe.com/reaction/1908086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-bromo-4-(tert-butyl)benzoateHCID 11959028—
ReactantHCID 178418546HCID 178418546—
CatalystSodium CyanideHCID 8929—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-tert-butyl-3-cyano-benzoateHCID 5855104243%

Reaction Conditions

Temperature110 °C

Reaction Steps

Methyl 3-bromo-4-tert-butyl-benzoate (2.26 g, 4.17 mmol) was dissolved in dry DMF (2.1 mL) before CuCN (821 mg, 9.17 mmol) and NaCN (1.0 mg, 0.021 mmol) were added. The mixture was flushed with nitrogen and was stirred at 110° C. for 24 h. The reaction mixture was diluted with ethyl acetate (70 mL) and was washed with water. The organics were dried over sodium sulfate and were evaporated to dryness. The crude material was purified by column chromatography eluting with 0-10% ethyl acetate in hexanes to give methyl 4-tert-butyl-3-cyano-benzoate (390 mg, 43%). ESI-MS m/z calc. 217.1. found 218.5 (M+1)+; Retention time: 2.07 minutes (3 min run). NMR (400 MHz, CD3CN) δ 8.31 (d, J=1.8 Hz, 1H), 8.16 (dd, J=8.4, 2.0 Hz, 1H), 7.72 (d, J=8.4 Hz, 1H), 3.92 (s, 3H), 1.55 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-e4359dd7273842e49c1c4f3ffc1b42bb
Source noteuspto-grants-2013_12