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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770592Generated: October 30, 2026

Triethylamine → Ethyl 2-(3-(tert-butyldimethylsilyloxy)benzylamino)-2-methylpropanoate

https://huagongshe.com/reaction/1770592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(t-Butyldimethylsilyloxy)benzaldehydeHCID 11207111—
ReactantEthyl 2-amino-2-methylpropanoate hydrochlorideHCID 22343822—
Solvent1,2-DichloroethaneHCID 11—
ProductEthyl 2-(3-(tert-butyldimethylsilyloxy)benzylamino)-2-methylpropanoateHCID 5952441790%

Reaction Steps

To 3-(tert-butyldimethylsilyloxy)benzaldehyde (Example 12-1c) (3.00 g, 12.7 mmol) in DCE (100 mL) was added ethyl 2-amino-2-methylpropanoate hydrochloride (25 mmol, ˜2 equiv.), molecular sieves 4A (5 g), and Et3N (2 equiv.). The mixture was stirred for 6 hours at room temperature and treated with NaBH(OAc)3 (2 equiv.). After the addition was completed, the reaction mixture was stirred overnight under nitrogen. The mixture was diluted with DMC (200 mL), carefully quenched with saturated aqueous NaHCO3 solution and the layers were separated. The aqueous phase was further extracted with DCM (2×100 mL). The combined organic extract was washed with water (50 mL), brine (100 mL) and dried over Na2SO4. The solvent was removed under vacuum and the residue was purified over silica gel using hexanes/EtOAc (2/8) to give ethyl 2-(3-(tert-butyldimethylsilyloxy)benzylamino)-2-methylpropanoate (4.02 g, 90%). MS 352 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09247759B2
Source datasetuspto-grants-2016_02
ORD IDord-1003b94cdbf84181b7d08f83e6444949
Source noteuspto-grants-2016_02