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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48172Generated: October 29, 2026

Methyl iodide → Methyl 2-[2-(2-methylpropyl)benzothiazol-5-yl]propionate

https://huagongshe.com/reaction/48172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethyl[2-(2-methylpropyl)benzothiazol-5-yl]acetateHCID 22742086—
ReactantEthylbenzene heptaneHCID 86759364—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-[2-(2-methylpropyl)benzothiazol-5-yl]propionateHCID 2274208898.7%

Reaction Steps

A solution of lithium diisopropylamide (2.0M solution in tetrahydrofran/ethylbenzene/heptane, 2.09 ml, 0.0042 mol) was added, dropwise, to a solution of methyl[2-(2-methylpropyl)benzothiazol-5-yl]acetate (1.1 g, 0.0042 mol) in tetrahydrofuran (27 ml) at −78° C. under a nitrogen atmosphere and the mixture was stirred at below −60° C. for 1 hour. Methyl iodide (2.29 ml, 0.037 mol) was added, dropwise, and the mixture was stirred at below −60° C. for a further 1 hour. The cooling bath was removed and the mixture was allowed to warm to room temperature over a period of 1 hour. The mixture was diluted with water, acidified with 2M aqueous hydrochloric acid and extracted with ethyl acetate. The organic extract was dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo to give methyl 2-[2-(2-methylpropyl)benzothiazol-5-yl]propionate (1.15 g) which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703347B2
Source datasetuspto-grants-2004_03
ORD IDord-344c3d98059b458586760dfa59c4605a
Source noteuspto-grants-2004_03