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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401891Generated: November 2, 2026

Ethyl Acetate → 4-[2-(4-Bromo-phenyl)-2-methoxycarbonyl-ethyl]-benzoic acid tert-butyl ester

https://huagongshe.com/reaction/1401891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-Bromo-2-methylphenyl acetateHCID 60026774—
Reactant4-Iodomethyl benzoic acid tert-butyl esterHCID 67212118—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(4-Bromo-phenyl)-2-methoxycarbonyl-ethyl]-benzoic acid tert-butyl esterHCID 67211347100%

Reaction Steps

A solution of 246.63 g of methyl-4-bromophenyl acetate and 342.54 g of 4-Iodomethyl benzoic acid tert-butyl ester in THF (1233 mL) was cooled to −8° C. A solution of lithium hexamethyl disilazide in THF (1185 mL, 1.0 M) was added dropwise ensuring that the temperature remaine below −2° C. After the addition was complete, the reaction was allowed to proceed for ˜45 min at the same temperature and then poured over a stirring mixture of ethyl acetate (2.46 L) and water (1.23 L). The organic phase was washed with saturated ammonium chloride and then with water. Dried over magnesium sulfate and concentrated under reduced pressure to obtain 450.5 g (100% yield) thick oil. HNMR: CDCl3, 1.41 (s, 9H), 2.88-2.90 (m, 1H), 3.24-3.28 (m, 1H), 3.45 (s, 3H), 3.63 (t, 1H). 6.96-6.99 (m, 4H), 7.25 (d, 2H), 7.68 (d, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907103B2
Source datasetuspto-grants-2014_12
ORD IDord-6d779bdda11245fc89438c93af105045
Source noteuspto-grants-2014_12