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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079186Generated: November 1, 2026

Benzyl Alcohol → HCID 53685280, compound

https://huagongshe.com/reaction/1079186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22872084HCID 22872084—
CatalystDimethylformamideHCID 6228—
SolventBenzeneHCID 241—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53685280HCID 536852808%

Reaction Steps

A 50 mL round bottom flask was charged with (+)-{4aR)-(10bR)-4-methyl-8-carboxy-10b-methyl-1,2,3,4,4a,-5,6,10b-octahydrobenzo[f]quinolin-3-one (100 mg, 0.37) and 2 mL of benzene. Oxalyl chloride (1.1 mmol) was added dropwise via syringe to the stirred mixture, followed by a catalytic amount of dimethylformamide (one drop). The mixture was allowed to stir at room temperature for 25 min, and then the volatiles were removed in vacuo. One mL of THF was added, followed by a solution of benzyl alcohol and pyridine (4 eq) in 1 mL of THF at 0°. It was then allowed to warm to room temperature, diluted with 50 mL of chloroform, and washed with 0.1N hydrochloric acid (2×25 mL), 10% sodium bicarbonate (2×25 mL), water, (2×25 mL), and brine (2×25 mL. The combined organic extracts were dried over sodium sulfate, concentrated and chromatographed on silica (ethyl acetate eluent), to give 11 mg (8%) of the title compound as an amorphous yellow foam. FDMS: m/e=349.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550134
Source datasetuspto-grants-1996_08
ORD IDord-12966ba5ebc846829b97fe52d53924ae
Source noteuspto-grants-1996_08