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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771036Generated: November 2, 2026

Triethylamine → t-butyl alpha-[5-(Boc-amino)-4-oxopentanoyloxy]-phenylacetate

https://huagongshe.com/reaction/1771036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 2-bromo-2-phenylacetateHCID 11000147—
Reactant5-((tert-Butoxycarbonyl)amino)-4-oxopentanoic acidHCID 17989820—
SolventEthyl AcetateHCID 8857—
Productt-butyl alpha-[5-(Boc-amino)-4-oxopentanoyloxy]-phenylacetateHCID 9003456978%

Reaction Steps

This compound was prepared from 5-(Boc-amino)-4-oxopentanoic acid (1.97 g; 8.5 mmol), the product of 6a (2.35 g; 8.7 mmol), and triethylamine (0.88 g; 8.7 mmol) in ethyl acetate (30 mL) as described in Example 1a. The crude product was purified by flash chromatography on a 65×55 mm silica gel 60 column eluted with ethyl acetate-hexane (1:2) (1100 mL) collecting 18×50 mL fractions. After evaporation of fractions 3-8, 2.79 g (78%) product was obtained (amber oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249086B2
Source datasetuspto-grants-2016_02
ORD IDord-04cef073c8344c4382c5d0542e83d501
Source noteuspto-grants-2016_02