HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15426387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,2-Cyclohexanedione | HCID 13006 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 22614273 | HCID 22614273 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15426387 | HCID 15426387 | — |
Reaction Steps
0.53 g (1.53 mmol) of 2-chloro-3-cyclohexanyloxymethyl-4-methylsulfonylbenzoic acid was treated with 2 drops of N,N-dimethylformamide and 0.59 g (4.58 mmol) of oxalyl chloride in 23 ml of methylene chloride and the mixture was refluxed for 2.5 h. It was then stripped off on a rotary evaporator, the residue was taken up in 23 ml of methylene chloride and the mixture was treated at 0° C. with 0.19 g (1.68 mmol) of cyclohexanedione and 0.46 g (4.58 mmol) of triethylamine. It was stirred at room temperature for 4 h. It was then concentrated on a rotary evaporator and purified by chromatography (silica gel, ethyl acetate:hexane=1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376429B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-e0890f92eccd48eab0ad056853376d64 |
| Source note | uspto-grants-2002_04 |