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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616997Generated: October 31, 2026

Triethylamine → Benzyl tert-butyl malonate

https://huagongshe.com/reaction/1616997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
Reactant1,1-Dimethylethyl N-(2-amino-2-oxoethyl)carbamateHCID 10910064—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductBenzyl tert-butyl malonateHCID 273671295.7%

Reaction Steps

Carbamoylmethyl-carbamic acid tert-butyl ester (8a; 0.84 g, 4.8 mmol) was dissolved in dichloromethane (10 mL), and added with triethylamine (1.0 mL, 7.2 mmol) and benzyl chloroformate (0.85 g, 0.75 mL, 5.0 mmol) at 0° C. After stirring for 5 min, 4-dimethylaminopyridine (DMAP; 0.32 g, 2.6 mmol) was added slowly with continuous stirring at 0° C. for 1 h. After the reaction is completed, dichloromethane (10 mL) and saturated Na2CO3 solution (10 mL) were added. The organic phase was washed by H2O (10 mL), 1N HCl (20 mL), H2O (20 mL) and saturated NaCl solution (20 mL) separately, and dried over MgSO4 and concentrated under reduced pressure to remove dichloromethane to obtain white solid product 12 (1.15 g; 95%). 1H-NMR (200 MHz) (CDCl3) δ: 7.30˜7.38 (m, 5H, ArH), 5.17 (s, 2H, CO2CH2Ph), 5.02 (br, s, 1H, NHBOC), 3.94 (d, 2H, Gly-H), 1.43 [s, 9H, CO2C(CH3)3]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765934B2
Source datasetuspto-grants-2014_07
ORD IDord-9edbb5fd57f94745ba1d1c2d4ac135e7
Source noteuspto-grants-2014_07