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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190702Generated: October 29, 2026

N-(tert-butoxycarbonyl)glycine → HCID 21904412, compound

https://huagongshe.com/reaction/2190702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 12376816HCID 12376816—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 21904412HCID 2190441269%

Reaction Steps

To a solution of Boc-glycine 130 (1.04 g, 5.88 mmol) and 4-bromobenzylethylamine 131 (1.00 g, 4.90 mmol) in CH2Cl2 (25 mL) at room temperature was added Hunig's base (1.30 mL, 7.35 mmol). The mixture was stirred at room temperature for 16 h. The mixture was poured into water (40 mL) and sat. NaHCO3 (3 mL), then extracted with CH2Cl2 (60 mL), washed with water (100 mL), and dried with Na2SO4. The residue was isolated by column chromatography (50/50/0.1 EtOAc/Hexane/NH4OH), to give 1.30 g of amide 132 as a white crystalline solid in 69% yield. 1H NMR (300 MHz, CDCl3, ppm): δ: 7.37 (d, J=7 Hz, 2H), 7.09 (d, J=7 Hz, 1H), 6.50 (s br, 1H), 5.15 (s br, 1H), 5.01-4.95 (m, 1H), 3.69 (d, J=6 Hz, 2H), 1.39 (d, J=7 Hz, 3H), 1.37 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324398B2
Source datasetuspto-grants-2012_12
ORD IDord-fa709816834c450b95ce0487cfa321e5
Source noteuspto-grants-2012_12