HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166361Generated: October 27, 2026
Triethylamine → 3-Cyano-4-methoxymethyl-5-phenoxy-beta-carboline
https://huagongshe.com/reaction/2166361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-Phenoxy-4-methoxymethyl-beta-carboline-3-carboxamide | HCID 23039409 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Cyano-4-methoxymethyl-5-phenoxy-beta-carboline | HCID 23039477 | 42.2% |
Reaction Steps
1.1 g of Br2 in 10 ml of methylene chloride is put in drop by drop into a stirred solution of 1.8 g (15 mmol) of triphenylphosphine in 50 ml of methylene chloride at 0° C. Then, 2 g of 5-phenoxy-4-methoxymethyl-beta-carboline-3-carboxamide and 1.9 ml of triethylamine are added. The reaction mixture is stirred for 1 hour at 0° C. and then vigorously stirred with 25 ml of methylene chloride and 25 ml of water for 5 minutes. After removal of the aqueous phase from the organic phase by concentration, 0.8 g of the desired product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04945090 |
|---|
| Source dataset | uspto-grants-1990_07 |
|---|
| ORD ID | ord-0a6a047c07b047d6914465e4502beddb |
|---|
| Source note | uspto-grants-1990_07 |
|---|