HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → benzyl N-(2-bromoethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl N-(2-bromoethyl)carbamate | HCID 278694 | 89% |
Reaction Steps
Benzyl chloroformate (26 mL, 0.176 mole) was added in one portion to a stirring mixture of bromoethylamine hydrobromide (44 g, 0.21 mole), triethylamine (64 mL, 0.46 mole), and methylene chloride (1 L) at below −40° C. After the addition, the cooling bath was removed, and the reaction was allowed to stir for 3 h. The mixture was transferred to a 2 L separatory funnel, and sequentially washed with water (2×500 mL), 2N HCl (250 mL), and water (500 mL). The resulting solution was suction filtered through a 100 g pad of silica gel and washed with methylene chloride. Evaporation of the solvents afforded the product 14 (40 g, 89%) as an oil. 1H NMR (300 MHz, CDCl3) δ 3.46 (t, 2H), 3.60 (q, 2H), 5.11 (s, 2H), 5.20 (br s, 1H), 7.35 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198286B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-530f4a4d66c744c4b4f4c3c61d263d19 |
| Source note | uspto-grants-2012_06 |