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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278059Generated: October 31, 2026

Hydrochloric Acid → HCID 13343383, compound

https://huagongshe.com/reaction/278059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
Reactantethyl (isopropylthio)acetateHCID 10773300—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13343383HCID 1334338356.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of diisopropylamine (15.4 mL, 0.11 mol) in tetrahydrofuran is cooled to 0° C., treated dropwise with a 2.04 M solution of n-butyllithium in tetrahydro-furan (51.4 mL, 0.105 mol), stirred at 0° C. for 30 minutes, treated dropwise with ethyl (isopropylthio)acetate (16.3 g, 0.1 mol), stirred at 0° C. for 1 hour, treated with methyl iodide (15.6 g, 0.11 mol), stirred at room temperature for 20 hours, and poured into an ice-water mixture (100 g) containing 15 mL of 6 N hydrochloric acid. The resulting aqueous mixture is extracted with ether. The combined organic extracts are washed sequentially with water, saturated sodium thiosulfate solution, water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a brown solution. Vacuum distillation of the brown solution gives the title product as a liquid (10.0 g) which is identified by NMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359009B1
Source datasetuspto-grants-2002_03
ORD IDord-602d2a9ccfa54643b5b62f3048cb3e1c
Source noteuspto-grants-2002_03