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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383939Generated: October 29, 2026

Ethyl Acetate → Ethyl (1-benzyl-4-hydroxyazepan-4-yl)acetate

https://huagongshe.com/reaction/383939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Benzyl-hexahydro-4H-azepin-4-oneHCID 1514350—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl (1-benzyl-4-hydroxyazepan-4-yl)acetateHCID 59291435—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of DIPA (3.1 mL) in THF (30 mL) was added dropwise a 2.6 M solution (8.6 mL) of n-butyl lithium in hexane at −70° C. After stirring at 0° C. for 40 minutes, EtOAc (2.3 mL) was added dropwise thereto at −70° C., followed by stirring for 5 minutes. A solution of 1-benzylazepan-4-one (3.6 g) in THF (10 mL) was added dropwise thereto, followed by stirring for 40 minutes. To the reaction mixture was added a saturated aqueous NH4Cl solution, followed by addition of water and extraction with EtOAc. The organic layer was washed with brine, dried over MgSO4, and then concentrated under reduced pressure. The residue was purified by medium-pressure preparative liquid chromatography (silica gel, YAMAZEN YFLC WPrep2XY, CHCl3:MeOH: aqueous ammonia) to obtain ethyl (1-benzyl-4-hydroxyazepan-4-yl)acetate (5.0 g) as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367696B2
Source datasetuspto-grants-2013_02
ORD IDord-66eee50a1cec47b39b7b99f201a7169b
Source noteuspto-grants-2013_02