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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271030Generated: November 2, 2026

1,2-Dichloroethane → Cocaine

https://huagongshe.com/reaction/271030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSuccinic anhydrideHCID 7922—
ReactantTriethylamineHCID 8471—
ReactantNorcocaine hydrochlorideHCID 3046136—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductCocaineHCID 446220—

Reaction Steps

A solution of norcocaine hydrochloride (1 g, 3.07 mmol), triethylamine (0.86 ml, 6.14 mmol) in methylene chloride (20 ml) is treated with succinic anhydride (614 mg, 6.14 mmol) and the mixture heated at 45.degree. C. overnight, as described in U.S. Pat. No. 5,876,727. The solvents are removed under reduced pressure and the residue purified using silica gel flash chromatography (2:1 chloroform:methanol as the eluent). This gives succinylated norcocaine (1.0 g, 84%) as a thick syrup (3.beta.-(Benzoyloxy)-8-succinoyl-8-azabicyclo[3.2.1]octane-2.beta.-carboxylic acid methyl ester). To a solution of the acid (14 mg, 0.036 mmol) in distilled water (1 ml) at 0.degree. C., EDC (10.4 mg, 0.055 mmol) was added. After 5 minutes a solution of Qβ VLP in PBS (1 ml) is added dropwise and the mixture is allowed to warm to ambient temperature overnight. The conjugate is purified by dialysis against PBS and the degree of conjugation analyzed by mass spectral analysis. The resultant conjugate is used to immunize individuals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452541B2
Source datasetuspto-grants-2008_11
ORD IDord-13a77ecef2a44988ba5a015340e28018
Source noteuspto-grants-2008_11