HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 87499731, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | 4-Chloro-3-(chlorosulfonyl)benzoyl chloride | HCID 15632689 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87499731 | HCID 87499731 | — |
Reaction Steps
To a solution of 4-chloro-3-(chlorosulfonyl)benzoyl chloride (1.0 g, 3.6 mmol) in DCM (10 ml) was added a solution of hydroxy ethyl morpholine (443 μl, 3.6 mmol) in DCM (1 ml). The reaction mixture was stirred for 12 h after which time no sulfonyl chloride was observed by LC-MS. Upon concentration of the crude reaction mixture a solid was isolated, which was trituated with ether to afford the desired compound as a brown solid. (1.54 g, 100%) IR (neat) vmax/cm−1 1724, 1174, 1450; δH (500 MHz, DMSO-d6) 8.49 (1H, d, 1.8 Hz), 7.97 (1H, dd, 8.2, 1.9 Hz), 7.56 (1H, d, 8.2 Hz), 4.38-5.00 (2H, m), 3.88-4.07 (2H, m), 3.76-3.83 (2H, m), 3.56-3.62 (2H, m), 3.36-3.54 (2H, m), 3.14-3.28 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115064B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-155d29f29e9d480bb8d879acb535bee8 |
| Source note | uspto-grants-2015_08 |