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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625886Generated: October 31, 2026

Nitrogen → HCID 90456988, compound

https://huagongshe.com/reaction/625886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 90457267HCID 90457267—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 90456988HCID 9045698861.1%

Reaction Steps

(S)-(9H-fluoren-9-yl)methyl 5-oxo-4-((m-tolyloxy)methyl)oxazolidine-3-carboxylate (825 mg, 1.921 mmol) was dissolved in CHCl3 (10 mL) and added triethylsilane (1.534 ml, 9.60 mmol) followed by TFA (10 ml, 130 mmol) and stirred at RT under positive pressure of N2 for 18 hrs. The reaction was then evaporated on rotovap until a sticky oil was left behind. The oil was dissolved in EtOAc and then extracted with sat. sodium bicarbonate (10 ml×2). There was a middle layer between the aqueous layer and organic layer that appeared to be the deprotonated product. The aqueous layer and middle layer were separated and collected and then acidified until pH 4-5. The solution formed a precipitate once acidic. EtOAc (200 ml) was used to extract the precipitate. The organic layer washed with brine, collected, dried over MgSO4, filtered and evaporated to get the pure product (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(m-tolyloxy)propanoic acid (506 mg, 1.173 mmol, 61.0% yield) as a white solid. ESI-MS (+) m/z=454 (M+Na)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308236B2
Source datasetuspto-grants-2016_04
ORD IDord-c74d401499d04074b1bee088c215387f
Source noteuspto-grants-2016_04