Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204159Generated: October 26, 2026

Hydrochloric Acid → 4-(2-Methoxyethoxy)-3-methylbenzoic acid

https://huagongshe.com/reaction/2204159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Hydroxy-3-methylbenzoic acidHCID 68138—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantPhosphonium, tetrabutyl-, hydroxide (1:1)HCID 84487—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Methoxyethoxy)-3-methylbenzoic acidHCID 585513706.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-hydroxy-3-methyl-benzoic acid (2.0 g, 13 mmol) in THF (24 mL) was added tetrabutylphosphonium hydroxide (18 mL of 40% w/v, 26 mmol). The reaction mixture was cooled to 0° C. in an ice water bath and then 1-bromo-2-methoxy-ethane (1.8 g, 1.2 mL, 13 mmol) was added. The reaction mixture was then allowed to warm to room temperature and stir overnight. The reaction mixture was made acidic by addition of 1M HCl and the reaction was extracted with ethyl acetate. The organics were dried over sodium sulfate and evaporated to yield 180 mg of 4-(2-methoxyethoxy)-3-methylbenzoic acid (yield: 6%). ESI-MS m/z talc. 210.2, found 209.2 (M-H)−. Retention time: 0.96 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-23ce4990c4d24dffb6bb4ee88f51982e
Source noteuspto-grants-2016_06