HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Carbamic acid, (4-oxobutyl)-, 9H-fluoren-9-ylmethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 58520747 | HCID 58520747 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Carbamic acid, (4-oxobutyl)-, 9H-fluoren-9-ylmethyl ester | HCID 22184307 | 98,000% |
Reaction Steps
To a stirring solution of N-Fmoc-4-amino-butyraldehyde diethyl acetal (0.050 mmol) in 1,4-dioxane (100 mL) was added aq. HCl (100 ml, 1:1 v/v, H2O: conc. HCl) and the reaction progress was monitored by MS. Upon completion, the organic solvent was removed by rotary evaporation, and the aqueous layer was extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with 5% NaHCO3 (2×75 mL), brine (75 mL), dried over Na2SO4, filtered and concentrated to dryness to yield the desired N-Fmoc-4-amino-butyraldehyde (15.35 g, 0.049 mol, 90.0% yield), which was carried through to the next step without further purification: MS m/e [M+Na]+ calcd 332.1, found 332.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524689B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-c746986bb8f64d6ebd5538084ebca13c |
| Source note | uspto-grants-2013_09 |