HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromopropylamine hydrobromide → Benzyl 3-bromopropylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromopropylamine hydrobromide | HCID 78701 | — |
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 3-bromopropylcarbamate | HCID 254436 | 92.1% |
Reaction Steps
TEA (6.91 g, 68.5 mmol) was added drop wise to an ice-cooled mixture of 3-bromopropylamine.hydrobromide (10.0 g, 45.6 mmol) and N-(Benzyloxycarbonyloxy)-succinimide (11.22 g, 47.9 mmol) in DCM (200 mL). The stirred mixture was allowed to warm to Rt overnight, then washed with water, brine, dried (MgSO4), filtered and concentrated, providing 11.43 g (92%) of N-(Benzyloxycarbonyl)-3-bromopropylamine, as a pale yellow oil. 1H NMR (CDCl3): 7.35 (m, 5H), 5.10 (s, 2H), 4.89 (br s, 1H), 3.44 (t, J=6.6 Hz), 3.35 (dd, J=12.9, 6.3 Hz, 2H), m (2.06, 2H). LCMS (LC: Hydrophobic/TFA, RT=6.4 min; MS: 294, 296 ([M+NH4]+, 22%), 272, 274 ([M+H]+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258259B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-8fd2d9e6c9eb4496954ef66c40393d73 |
| Source note | uspto-grants-2012_09 |