HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379232Generated: October 30, 2026
Potassium bisulfate → tert-butyl N-(3-oxobutyl)carbamate
https://huagongshe.com/reaction/379232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | tert-butyl N-(2-(methoxy(methyl)carbamoyl)ethyl)carbamate | HCID 10823469 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-butyl N-(3-oxobutyl)carbamate | HCID 12111481 | — |
Reaction Steps
A solution of BOC-beta-alanine (20 g, 105 mmol), 10-2 (10.3 g, 105 mmol), BOP reagent (46.5 g, 105 mmol), and N-methylmorpholine (46 mL, 420 mmol) in acetonitrile (500 mL) was stirred for 15 h. The reaction was diluted with EtOAc, washed with H2O, 10% KHSO4(aq.), sat. NaHCO3, dried (MgSO4) and concentrated to give crude [2-(methoxy-methyl-carbamoyl)-ethyl]-carbamic acid tert-butyl ester 10-3 as a yellow oil. TLC Rf=0.42 (silica, 20% EtOAc/hexanes). To a solution of this crude amide in THF (500 mL) at 0° C. was added CH3MgBr (100 mL of 3M in ether, 300 mmol) over 30 minutes. After 2 h, 10% KHSO4(aq.) was added, the mixture warmed to 25° C., and diluted with EtOAc. The organics were washed with sat. NaHCO3, dried (MgSO4) and concentrated. Flash chromatography (silica, 20% EtOAc/hexanes) gave 10-4 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06297249B1 |
|---|
| Source dataset | uspto-grants-2001_10 |
|---|
| ORD ID | ord-200fc078e9cc49868a7c437203d9c473 |
|---|
| Source note | uspto-grants-2001_10 |
|---|