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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410639Generated: October 29, 2026

4-(Heptyloxy)benzoyl chloride → 4-(2-(((Benzyloxy)carbonyl)amino)-3-(tert-butoxy)-3-oxopropyl)-2-methoxyphenyl 4-(heptyloxy)benzoate

https://huagongshe.com/reaction/2410639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Heptyloxy)benzoyl chlorideHCID 2724182—
ReactantTert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoateHCID 58545693—
SolventDichloromethaneHCID 6344—
Product4-(2-(((Benzyloxy)carbonyl)amino)-3-(tert-butoxy)-3-oxopropyl)-2-methoxyphenyl 4-(heptyloxy)benzoateHCID 5854580375%

Reaction Steps

Prepared using General Procedure 3: To a stirred solution of tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoate INT-2 (4.7 g, 11.71 mmol) and TEA (3.05 mL, 21.07 mmol) in DCM (50 mL) at 0° C. was added 4-(heptyloxy)benzoyl chloride (2.95 mL, 12.29 mmol) dropwise. After warming to room temperature and stirring for 10 min, the mixture was quenched with saturated aqueous NaHCO3 (50 mL) and water (50 mL). The organic layer was dried over MgSO4 and concentrated. The product was purified by chromatography (EA/hexanes) to afford 5.46 g (75%) of 4-(2-(((benzyloxy)carbonyl)amino)-3-(tert-butoxy)-3-oxopropyl)-2-methoxyphenyl 4-(heptyloxy)benzoate INT-3. LCMS-ESI (m/z) calculated for C36H45NO8: 619. Found 564 [M+H-tBu]+, tR=3.22 min (Method 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816121B2
Source datasetuspto-grants-2014_08
ORD IDord-b8d7b20c93684f818d55748b172fdb60
Source noteuspto-grants-2014_08