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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775802Generated: October 26, 2026

4-tert-Butylbenzoyl chloride → HCID 73939388, compound

https://huagongshe.com/reaction/1775802

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-Butylbenzoyl chlorideHCID 74372—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-methyl 2-amino-3-(4-cyanophenyl)propanoateHCID 54521608—
SolventDichloromethaneHCID 6344—
ProductHCID 73939388HCID 7393938888%

Reaction Steps

Prepared using General Procedure 3: To the solution of (S)-methyl 2-amino-3-(4-cyanophenyl)propanoate (789.2 mg, 3.32 mmol) in DCM (15 mL) and DIEA (1.29 g, 9.96 mmol) was added 4-(tert-butyl)benzoyl chloride (981.3 mg, 4.99 mmol) at room temperature. The reaction was stirred for 2 h and the reaction was partitioned between DCM and saturated aqueous NaHCO3. The organic layer was dried over mgSO4 and concentrated. The crude product was purified by chromatography (EA/hexanes) to afford 1.06 g (88%) of (S)-methyl 2-(4-(tert-butyl)benzamido)-3-(4-cyanophenyl)propanoate. LCMS-ESI (m/z calculated for C22H24N2O3: 364.2. found 365.3 [M+H]+, tR=3.55 min (Method 1). 1H NMR (400 MHz, CDCl3) δ 8.81 (d, J=8.0 Hz, 1H), 7.85-7.60 (m, 4H), 7.49 (dd, J=15.1, 8.4 Hz, 4H), 4.85-4.60 (m, 1H), 3.65 (s, 3H), 3.30-3.23 (m, 1H), 3.18 (dd, J=13.7, 10.6 Hz, 1H), 1.29 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260427B2
Source datasetuspto-grants-2016_02
ORD IDord-250888268fad46b3b61e1b5584545bdb
Source noteuspto-grants-2016_02