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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429762Generated: November 1, 2026

Hydrochloric Acid → HCID 71459160, compound

https://huagongshe.com/reaction/1429762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 71450167HCID 71450167—
CatalystIron(3+) ethanedioate--water (2/3/6)HCID 57370413—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 71459160HCID 7145916048%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of iron(III) oxalate hexahydrate (79.4 mg, 0.13 mmol, 30 equiv) in H2O (22 mL) was cooled to 0° C. and air was bubbled through the mixture for 10 minutes. A solution of 10′-methoxyanhydro-vinblastine (22a, 4.5 mg, 0.0055 mmol, 1 equiv) in H2O (0.5 mL), aqueous 0.1 N HCl (0.5 mL), and CF3CH2OH (0.1 mL) was transferred by pipette to the mixture and NaBH4 (4.1 mg, 0.11 mmol, 20 equiv) in H2O (1 mL) was added to the mixture at 0° C. The resulting mixture was stirred for 30 min before being quenched by addition of 28-30% aqueous NH4OH (10 mL). The mixture was extracted with 10% MeOH in CH2Cl2 and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. PTLC (SiO2, Et3N:MeOH:EtOAc=3:3:97) provided 10′-methoxyvinblastine (22b, 2.2 mg, 0.0026 mmol, 48%) as a white solid and 10′-methoxyleurosidine (1.3 mg, 0.0015 mmol, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940754B2
Source datasetuspto-grants-2015_01
ORD IDord-67c1e353b31b4c1c81858fa06e0f5daf
Source noteuspto-grants-2015_01