HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropylamine → HCID 19868194, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Pyruvate | HCID 107735 | — |
| Reactant | 2-Ketobutyrate | HCID 3593277 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | HCID 178418750 | HCID 178418750 | — |
| Product | HCID 19868194 | HCID 19868194 | — |
| Product | HCID 86743742 | HCID 86743742 | — |
Reaction Steps
All reactions were carried out in an atmosphere of dry nitrogen using standard Schlenk-techniques (Manipulations of air-sensitive compounds, D. F. Shriver, editor Mc. Graw Hill, N.Y., 1969). Solvents were distilled from sodium prior to use. N-t-butyliminoethylglyoxylate and N-i-propyliminomethylglyoxylate were prepared in a condensation reaction; cf. t-butylamine and i-propylamine with ethylglyoxylate and methylglyoxylate respectively. 2,2,5,5-tetramethyl-1-aza-2,5-disilylacyclopentane-1-acetic acid ethyl ester has been described in Tetrahedron Lett., 22, 1787 (1981). Solutions of n-butyllithium in n-hexane and diethylzinc in n-hexane are commercially available.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04898955 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-c436a75a199446beb0a7e67b3752543b |
| Source note | uspto-grants-1990_02 |