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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486692Generated: October 30, 2026

Dimethyl Sulfate → N-Formyl-2-methoxy-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamine

https://huagongshe.com/reaction/486692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantN-formyl-2-hydroxy-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamineHCID 22414398—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductN-Formyl-2-methoxy-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamineHCID 2241440865.3%

Reaction Steps

To an ice-water chilled solution of 5.10 g of N-formyl-2-hydroxy-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine and 100 ml of tetrahydrofuran, was added 2.24 g of potassium t-butoxide and then a solution of 2.52 g of dimethylsulfate and 25 ml of tetrahydrofuran dropwise, with stirring. The mixture was stirred at ice-bath temperature for 30 min, at room temperature for one hr, and at reflux for 30 mins. Additional dimethylsulfate and potassium t-butoxide were added and the mixture was refluxed for 20 min. The reaction mixture was decanted into 40 ml of water and basified with 10% sodium hydroxide solution. The mixture was extracted with dichloromethane. The combined organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was combined with a previous sample. The combined residue was purified by preparative HPLC (Water Associates Prep LC/System 500, silica gel, material applied as a solution in dichloromethane, eluted with ethyl acetate-hexane (1:1, 200 ml/min flow rate). The appropriate fractions were combined and concentrated. The residue crystallized during refrigerated storage. Recrystallization from cyclohexane afforded 3.5 g of the product, mp 80°-83° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292760
Source datasetuspto-grants-1994_03
ORD IDord-3f4e4c4ab6284d418a0973405bc6f09a
Source noteuspto-grants-1994_03