HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butanesulfinamide → Ethyl 6-((tert-butylsulfinyl)imino)hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | Ethyl 6-oxohexanoate | HCID 11171124 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 6-((tert-butylsulfinyl)imino)hexanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-8f62a4ac96a54066ade31d30cf61ccf2 |
| Source note | uspto-grants-2016_01 |