HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20285488, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanethioic acid, S-(3-chloro-2-methyl-3-oxopropyl) ester | HCID 103458 | — |
| Reactant | N-Cycloheptylglycine 1,1-dimethylethyl ester | HCID 20285438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20285488 | HCID 20285488 | 98.7% |
Reaction Steps
To a stirred and chilled (0°-5° C.) solution of N-cycloheptylglycine t-butyl ester (32.9 g, 0.12 mol) and triethyl amine (13.2 g, 0.13 mol) in methylene chloride (150 ml) was added dropwise 3-acetylthio-2-methylpropanoyl chloride (21.6 g, 0.12 mol) dissolved in 50 ml methylene chloride. The reaction mixture was stirred overnight. Filtration of the reaction mixture followed by washing the filtrate with saturated sodium bicarbonate (500 ml), brine (500 ml), 5% HCL (4×500 ml), brine (500 ml), saturated aqueous sodium bicarbonate (3×500 ml), brine (500 ml); drying the organic layer over Na2SO4 and MgSO4 ; filtration; and solvent evaporation afforded a nearly quantitative yield of the desired compound (44 g, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256761 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-640364a04e4345e8bc3a096ecf87f2b8 |
| Source note | uspto-grants-1981_03 |