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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737450Generated: October 26, 2026

N-Methylphenylethanolamine → HCID 21842621, compound

https://huagongshe.com/reaction/1737450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylphenylethanolamineHCID 913—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantDiisopropylethylamineHCID 81531—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21842621HCID 21842621—

Reaction Steps

A solution of α-(methylaminomethyl)benzyl alcohol (1.00 g, 6.61 mmol) in 15 mL of THF was cooled in an ice bath. Benzenesulfonyl chloride (0.886 mL, 1.23 g, 6.94 mmol) and N,N-diisopropylethylamine (2.3 mL, 1.7 g, 13 mmol) were added and mixture was allowed to warm to room temperature. After 30 min, the solvent was evaporated and the residue was partitioned between 50 mL of ethyl acetate and 40 mL of saturated aqueous sodium bicarbonate. The aqueous layer was extracted with 2×50 mL of ethyl acetate. The combined organic layers were washed with 50 mL of brine, dried over sodium sulfate, and evaporated. Purification by flash column chromatography on silica gel, eluting with 20-50% ethyl acetate in hexane, gave the title compound in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962462
Source datasetuspto-grants-1999_10
ORD IDord-ba598985bff041bf90162b74bd66b628
Source noteuspto-grants-1999_10