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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658759Generated: October 25, 2026

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

https://huagongshe.com/reaction/658759

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 numberUS08076491B2
Source datasetuspto-grants-2011_12
ORD IDord-6fac7cb26a0942f499fedb498f71093a
Source noteuspto-grants-2011_12