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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167206Generated: October 26, 2026

Water → Methyl 2-(4-t-butylphenyl)propanoate

https://huagongshe.com/reaction/1167206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantMethyl p-tert-butylphenylacetateHCID 605629—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4-t-butylphenyl)propanoateHCID 10704172101%

Reaction Steps

23.3 mL of lithium bis(trimethylsilyl)amide (1.0 M, 23 mmols) was added dropwise to 4.75 g (23 mmol) of methyl 4-tert-butylphenylacetate in 100 mL of dry THF at −78° C. while stirring under nitrogen. The mixture was stirred at this temperature for 45 minutes, then 1.5 mL (24 mmol) methyl iodide was added dropwise and the solution was stirred for an additional 1 hour at −78° C. The mixture was poured into 200 mL of H2O and the desired product was extracted with 500 mL diethyl ether. The organic layer was backwashed once with 500 mL H2O, dried over K2CO3, and concentrated under reduced pressure to yield 5.12 g of a dark oil. The oil was purified via silica gel chromatography eluting with a solvent gradient of hexanes to hexanes/ethyl acetate 19:1. The fractions containing the desired product were combined and concentrated under reduced pressure to yield the title compound 2.65 g (53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617351B1
Source datasetuspto-grants-2003_09
ORD IDord-80d728f4368f4aac95bef45f2ed68013
Source noteuspto-grants-2003_09