HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → HCID 12649781, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 12649780 | HCID 12649780 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12649781 | HCID 12649781 | — |
Reaction Steps
A mixture of 6.6 g. (0.028 mole) of 7-fluoro-2-carbethoxy-1,2,3,4-tetrahydropyrrolo[3,4-b]indole, 8.86 g. (0.031 mole) of cuprous bromide, 3.28 g. (0.031 mole) of sodium carbonate and 17.2 g. (0.098 mole) of p-bromofluorobenzene in 75 ml. of N-methyl-2-pyrrolidione is heated to reflux for 4 hrs. The reaction mixture is cooled and poured into ice and water containing 40 ml. of ethylene diamine. The mixture is extracted with benzene, and the benzene extracts subsequently back-washed with water and a saturated brine solution and dried over magnesium sulfate. Removal of the solvent in vacuo provides a gum which on trituration with hexane provides 5.8 g. of product as a brown solid, m.p. 143°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006164 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-d4902f8917f04d2aa69faab7b8a76c34 |
| Source note | uspto-grants-1977_02 |