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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414891Generated: November 4, 2026

Hydrochloric Acid → HCID 10158751, compound

https://huagongshe.com/reaction/2414891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-BromopropaneHCID 6358—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 10270645HCID 10270645—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 10158751HCID 10158751—

Reaction Conditions

Temperature60 °C

Reaction Steps

42ELH89 (0.25 g, 0.67 mmol, 1.0 eq) was transferred to a 4 ml vial and dissolved in acetonitrile (2 ml). Isopropyl bromide (0.25 g, 3.0 eq.) was added along with Hünigs base (0.87 g, 10.0 eq.). The vial was sealed and shaken for 4 days at 60° C. The reaction mixture was transferred to a separatory funnel with distilled water and CH2Cl2. The aqueous phase was made basic with sodium hydrogen carbonate and extracted with dichloromethane (3 times). The organic layers were collected and dried with sodium sulfate and concentrated, this resulted in a yellow oil. The product was purified by flash chromatography (3% MeOH in CH2Cl2). The resulting product was dissolved in dichloromethane (1 ml) and HCl (1 eq. 2 M HCl in ether) was added under stirring. The salt precipitated by addition of the dichloromethane solution into heptane. Concentration on the rotary evaporator returned the product as white crystals. Yield 101.2 mg (63%), UV/MS 94/96 (M+ 415), Rf 0.25 (3% MeOH/CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815458B2
Source datasetuspto-grants-2004_11
ORD IDord-4b49de507fd24ae29e0e9d94dedff243
Source noteuspto-grants-2004_11