HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethylamine hydrobromide → 1,8-Diamino-3-oxa-6-azaoctane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Reactant | 2,2'-Oxybis(ethylamine) hydrochloride | HCID 2829023 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,8-Diamino-3-oxa-6-azaoctane | HCID 19973832 | — |
Reaction Steps
To a mixture of 2,2'-oxy-bis(ethylamine)dihydrochloride (1) (177 mg, 1 mmol), bromoethylamine hydrobromide (2) (204.9 mg, 1 mmol), in ethanol (10 mL) was added sodium methoxide (162.6 mg, 3 mmol) at room temperature. The reaction mixture was refluxed for 48 hours under a positive flow of argon. Reaction mixture was cooled to room temperature, ethanol was evaporated on rotavapor and the crude product (135 mg) was directly taken into next step to prepare the bis-naphthalimide, compound 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561042 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-b8bac8ae5b584f38b78e6952feed6e86 |
| Source note | uspto-grants-1996_10 |