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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410638Generated: November 3, 2026

Benzyl chloroformate → Tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoate

https://huagongshe.com/reaction/2410638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantTert-butyl 2-amino-3-(4-hydroxy-3-methoxyphenyl)propanoateHCID 58545613—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoateHCID 5854569359%

Reaction Steps

Prepared using General Procedure 2: To a stirred solution of tert-butyl 2-amino-3-(4-hydroxy-3-methoxyphenyl)propanoate INT-1 (5.29 g, 19.8 mmol) and TEA (4.29 mL, 29.7 mmol) in DCM (50 mL) at 0° C. was treated with benzyl carbonochloridate (3.00 mL, 21.1 mmol) dropwise over 5 min. After stirring for 10 min, the mixture was washed with 1M HCl (150 mL), dried over MgSO4, and concentrated. The residue was taken up in MeOH (20 mL) and treated with 2 N NaOH (5 mL). After 10 min, the mixture was acidified and the product was purified by chromatography (EA/hexanes) to afford 4.7 g (59%) of tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoate INT-2. LCMS-ESI (m/z) calculated for C22H27NO6: 401. Found 424 [M+Na]+, tR=2.47 min (Method 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816121B2
Source datasetuspto-grants-2014_08
ORD IDord-69d21f8dc29e492cb2c64e9d5b7ba0c5
Source noteuspto-grants-2014_08