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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838095Generated: November 2, 2026

Benzenepropanoyl chloride → HCID 12112436, compound

https://huagongshe.com/reaction/1838095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenepropanoyl chlorideHCID 64801—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2-Amino-4-fluorophenyl)methanolHCID 12737325—
SolventDichloromethaneHCID 6344—
ProductHCID 12112436HCID 1211243687.8%

Reaction Steps

To a solution of 2-amino-4-fluorobenzyl alcohol from Step 1 (2.00 g, 14.17 mmol) and methylene chloride (45 mL), was added N,N,-diisopropylethylamine (3.70 g, 28.34 mmol) followed by hydrocinnamoyl chloride (4.78 g, 28.34 mmol) dropwise over 15 min under an argon atmosphere at 23° C. After 16 h, the reaction was diluted with methylene chloride (100 mL), washed with KHSO4 (1 N, 1×80 mL), sat'd NaHCO3 (1×80 mL), brine (1×80 mL) and dried (MgSO4). After concentration in vacuo, the crude residue was dissolved in methanol (14 mL) and NaOH (1.5 N, 14 mL) was added at 23° C. under argon. After 2 h at 23° C., the reaction was concentrated in vacuo, diluted with ether (150 mL), washed with brine (100 mL), and dried (MgSO4). After concentration in vacuo, the residue was purified by flash chromatography (ethyl acetate:hexane 1:3) to afford N-[5-fluoro-2-hydroxymethylphenyl]benzenepropanamide (3.40 g, 87.8%) as an oil: 1H NMR (CDCl3) δ2.65 (t, J=7 Hz), 3.05 (t, J=7 Hz), 4.48 (s), 6.68-6.74 (m), 7.00-7.34 (m), 7.83-7.91 (m) 8.72 (br s). MS (EI) 273, 255, 212. IR (neat) 3500-3150, 1667 cm−1. Anal. Calc'd. for C16H16NO2F: C, 70.31; H, 5.90; N, 5.13. Found: C, 70.26; H, 6.11; N, 5.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673788B2
Source datasetuspto-grants-2004_01
ORD IDord-1ed7dc8b77644a1aaa5b3345d4a316d2
Source noteuspto-grants-2004_01