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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243130Generated: October 25, 2026

Methyl iodide → 8-Methoxy-2-methyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1243130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 8-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058286—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexamethylphosphoramideHCID 12679—
Product8-Methoxy-2-methyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl esterHCID 6958512184%

Reaction Steps

To iPr2NH (202 mg, 2.0 mmol) in THF (1.0 mL) was added BuLi (2.5 M, 0.8 mL, 2.0 mmol) at −78° C. After 10 minutes, 8-methoxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl ester in THF (1.0 mL) was added and the reaction mixture turned yellow. Methyl iodide (568 mg, 4.0 mmol) and HMPA (1.0 mL) were added after 30 minutes. The reaction mixture was allowed to stir at −78° C. for 3 hours at ambient temperature before aqueous NH4Cl was added. The mixture was extracted with ethyl acetate (3×20 mL) and the combined extracts were dried over MgSO4 and purified by column chromatography to give 8-methoxy-2-methyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl ester (170 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115767B2
Source datasetuspto-grants-2006_10
ORD IDord-8bbe002405d94a3e9158b9eabddb9607
Source noteuspto-grants-2006_10