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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393106Generated: November 2, 2026

Dimethylformamide → HCID 54447215, compound

https://huagongshe.com/reaction/2393106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-3,3-dimethylpentanoic acid hydrochlorideHCID 71344521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54447215HCID 544472154.1%

Reaction Steps

2-amino-3,3-dimethylpentanoic acid hydrochloride (1.63 g), (JCS Chem. Comm. 11, 830-1992) is mixed with diisopropylethylamine (3.6 g, 3.1 equivalent) in dry THF (100 mL). The 4-methoxybenzenesulfonyl chloride (1.86 g, 1 equivalent) is added as a solid. DMF (25 mL) is added to the resulting suspension. After stirring overnight at room temperature the solvents are removed under vacuum. The residue is partitioned between ethyl acetate (200 mL) and 1N HCl (100 mL). The organic phase is separated and the aqueous phase extracted with several more portions of ethyl acetate. The combined organic phases are washed with 1N HCl and then brine. The organic phase are dried (MgSO4), filtered, and concentrated under reduced pressure. The resulting crude product is loaded onto a reverse phase column as a DMSO solution. The column is eluted using a step gradient (10% increments), starting with 30% acetonitrile/water and ending at 90% acetonitrile/water. Combination of the appropriate fractions gave 116 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05804593
Source datasetuspto-grants-1998_09
ORD IDord-d8f0ddf7cbc74d4eb4fc66e62bd1baf9
Source noteuspto-grants-1998_09