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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330068Generated: October 30, 2026

Pivaloyl chloride → HCID 14328129, compound

https://huagongshe.com/reaction/330068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
Reactant2-Chloroethylamine hydrochlorideHCID 9793737—
ReactantHCID 23200466HCID 23200466—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 14328129HCID 1432812987.9%

Reaction Steps

Triethylamine (3.50 ml, 25 mM) was added to compound 037 (4.90 g, 25 mM) dissolved in tetrahydrofuran (50 ml) and pivaloyl chloride (3.05 g, 25 mM) was added dropwise at -5° C., then the mixture was stirred for 30 minutes. Chloroform (50 ml) in solution with 2-chloroethylamine hydrochloride (2.90 g, 25 mM) and triethylamine (3.9 ml, 28 mM) was added dropwise thereto, then the mixture was stirred for 4 hours while slowly reaching room temperature. The reaction mixture was concentrated in vacuo, the residue was dissolved in chloroform and washed with dilute aqueous potassium carbonate. The aqueous layer was extracted with chloroform. The organic layer was combined, dried with anhydrous magnesium sulfate, and concentrated in vacuo. The residue was charged on a column of silica gel (C-200, 40 g), and eluted successively with chloroform and chloroformmethanol (20:1) to obtain the product (5.66 g, yield: 7.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894453
Source datasetuspto-grants-1990_01
ORD IDord-3a35f0d906e34dfcb139126f857df4f2
Source noteuspto-grants-1990_01