HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → (s)-2-Amino-n-(2-mercapto-ethyl)-3-methyl-butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 87903836 | HCID 87903836 | — |
| Product | (s)-2-Amino-n-(2-mercapto-ethyl)-3-methyl-butyramide | HCID 3078315 | — |
Reaction Steps
To 26g (222.0 mg, 0.80 mmol) in a 100 mL round-bottom flask purged with argon were added CH2Cl2 (2.00 mL, 31.2 mmol), triethylsilane (1.28 mL, 8.0 mmol), and trifluoroacetic acid (616 μL, 8.0 mmol). The reaction was stirred for 2.5 hours at room temperature, then concentrated in vacuo. The crude product was purified by silica gel chromatography using 10% methanolic CH2Cl2 as eluant. Clean fractions were combined, and concentrated in vacuo to afford 27g as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07045360B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-c0abe223325448de87a4995e6244ac11 |
| Source note | uspto-grants-2006_05 |