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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594325Generated: November 1, 2026

Tert-Butanesulfinamide → Ethyl 6-((tert-butylsulfinyl)imino)hexanoate

https://huagongshe.com/reaction/594325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButanesulfinamideHCID 3382465—
ReactantEthyl 6-oxohexanoateHCID 11171124—
CatalystCopper SulfateHCID 24462—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-((tert-butylsulfinyl)imino)hexanoateHCID 86695621—

Reaction Steps

A yellow solution of ethyl 6-oxohexanoate (44.80 mmol) in DCM (92 ml) was treated with 2-methylpropane-2-sulfinamide (5.431 g; 44.80 mmol) and with anh. CuSO4 (14.302 g; 89.61 mmol). The resulting beige heterogeneous mixture was further stirred at rt, under nitrogen, for 24 h. The resulting heterogeneous mixture was then filtered over a short pad of celite, and the separated solids were further washed with DCM. The obtained orange filtrate was concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH=25/1) afforded ethyl 6-((tert-butylsulfinyl)imino)hexanoate as a yellow/orange oil. LC-MS (conditions B): tR=0.81 min.; [M+H]+: 262.07 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-8f62a4ac96a54066ade31d30cf61ccf2
Source noteuspto-grants-2016_01