HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-Bromoacetyl-S-triphenylmethyl-L-cysteine ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | S-trityl-cysteine ethyl ester | HCID 21144450 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Bromoacetyl-S-triphenylmethyl-L-cysteine ethyl ester | HCID 57318726 | 69% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of S-triphenylmethyl-L-cysteine ethyl ester (18 g, 46 mmol.) and triethylamine (6.4 mL, 46 mmol.) in dry THF (250 mL) under nitrogen was cooled to 0° C. A solution of bromoacetyl bromide (9.28 g, 46 mmol.) in dry THF (60 mL) was added dropwise during which time the solution turned cloudy. The reaction mixture was stirred at 0° C. for 1 h and then at room temperature for 1 h. The reaction mixture was filtered and the filtrate was concentrated in vacuo to give an oil. The oil was partitioned between methylene chloride and water (60 mL each), the organic layer washed with 5% HCl, NaHCO3, dried (magnesium sulfate), filtered, and the volatiles removed to give the desired product (69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06022523 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-99e1d454d0384ee4a57b68b1ad558de0 |
| Source note | uspto-grants-2000_02 |