HuagongsheHuagongshe Chemistry Print Report · For research reference only
(-)-cis-1,2-Dimethoxy-4-(2-aminocyclohexyl)benzene → HCID 53795669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (-)-cis-1,2-Dimethoxy-4-(2-aminocyclohexyl)benzene | HCID 14321190 | — |
| Reactant | HCID 18621299 | HCID 18621299 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 53795669 | HCID 53795669 | 94.2% |
Reaction Steps
3.0 g of (−)-cis-1,2-dimethoxy-4-(2-aminocyclohexyl)benzene (compound C2) are dissolved in 100 ml of methylene chloride and 3.0 ml of triethylamine. A solution of 3.0 g of 4-(2-ethyl-2-H-tetrazol-5-yl)benzoyl chloride in 50 ml of methylene chloride is added dropwise at RT and the mixture is extracted, after stirring for 2 h, with 100 ml each of water, 2N hydrochloric acid, satd. sodium hydrogencarbonate solution and water again. The organic phase is dried using sodium sulphate and concentrated. The residue is taken up in petroleum ether (low)/ethyl acetate in the ratio 2/1, filtered off with suction and dried. 5.2 g of the title compound of m.p. 188-192° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06534519B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-8fbf437fd4dc473ba7c9a2392f080fe3 |
| Source note | uspto-grants-2003_03 |