HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Boc-DTrp-OBzl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-((tert-Butoxy)carbonyl)-D-tryptophan | HCID 111050 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Boc-DTrp-OBzl | HCID 10739405 | 95% |
Reaction Steps
To an ice-cooled solution of Boc-D-Trp-OH (8.61 g) in DMF (100 ml) were added benzyl bromide (7.19 g) and diisopropylethylamine (4.02 g). The solution was stirred for two hours at the same temperature and overnight at room temperature. After evaporation, the residue was extracted with ethyl acetate. The organic layer was washed successively with water, sodium hydrogencarbonate solution, 0.5 hydrochlolic acid, and sodium chloride solution, and dried over magnesium sulfate. Evaporation gave Boc-D-Trp-OBzl (10.6 g) as a crystalline mass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05187156 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-b08df90ed268472484e2250dbf5f4ea9 |
| Source note | uspto-grants-1993_02 |