Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496763Generated: October 30, 2026

Propylamine → Propyl pentanesulfonamide

https://huagongshe.com/reaction/496763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylamineHCID 7852—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Pentanesulfonyl chlorideHCID 237555—
SolventDichloromethaneHCID 6344—
ProductPropyl pentanesulfonamideHCID 2232263895%

Reaction Conditions

Temperature0 °C

Reaction Steps

Pentane sulfonyl chloride (687 mg, 4.03 mmol) was dissolved in 5 mL CH2Cl2 and added to an ice-cooled solution of n-propylamine (0.40 mL, 4.82 mmol) and ethyldiisopropylamine (0.85 mL, 4.88 mmol) in 5 mL CH2Cl2 under a nitrogen atmosphere. The reaction was stirred at 0° C. for 30 min, then at 25° C. for 4 h. The solution was partitioned between 20 mL of 1.0 M aqeous NaHSO4 and 25 mL CH2Cl2. The organic phase was washed sequentially with 25 mL H2O and 25 mL brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide 739 mg (3.83 mmol, 95%) of the title compound as a white solid. TLC (25% EtOAc-hexane) Rf 0.23; 1H NMR (CDCl3, 300 MHz) δ 0.92 (t, J=7 Hz, 3H), 0.97 (t, J=7 Hz, 3H), 1.28-1.50 (br m, 4H), 1.52-1.68 (m, 2H), 1.75-1.90 (br m, 2H), 2.98-3.06 (m, 2H), 3.08 (q, J=6 Hz, 2H), 4.10-4.23 (br m, 1H); MS (DCl/NH3) m/e 211 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946481B1
Source datasetuspto-grants-2005_09
ORD IDord-9ff45ba4ca86428bb9b0f1bdd5509521
Source noteuspto-grants-2005_09