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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354452Generated: November 1, 2026

Tetrabutylammonium Fluoride → trans-1-tert-butoxycarbonyl-4-dimethylamino-(2S)-hydroxymethylpyrrolidine

https://huagongshe.com/reaction/354452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactanttrans-1-tert-butoxycarbonyl(2S)-(tert-butyldiphenylsilyloxy)methyl-4-dimethylaminopyrrolidineHCID 69334202—
SolventTetrahydrofuranHCID 8028—
Producttrans-1-tert-butoxycarbonyl-4-dimethylamino-(2S)-hydroxymethylpyrrolidineHCID 20737863108.3%

Reaction Steps

To a stirred solution of trans-1-tert-butoxycarbonyl(2S)-(tert-butyldiphenylsilyloxy)methyl-4-dimethylaminopyrrolidine (330 mg, 0.68 mmol) in THF (5 ml) was added TBAF (1.0 M solution in THF, 1.0 ml, 1.0 mmol) at 0° C. The reaction mixture was stirred at room temperature for 2 hr. The mixture was concentrated in vacuo. The residue was purified by column chromatography on silica gel with MeOH—CH2Cl2 (3:97 to 20:80, v/v) as eluent to give trans-1-tert-butoxycarbonyl-4-dimethylamino-(2S)-hydroxymethylpyrrolidine (180 mg, quant) as a pale yellow oil. 1H-NMR (CDCl3) δ1.47 (s, 9H), 2.23 (s, 6H), 1.65-1.75 (m, 2H), 2.75-4.10 (m, 4H), 3.61 (d, J=5.6 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-c2d594a8cc04430ca7579a1ca932f7b1
Source noteuspto-grants-2004_06