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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911540Generated: October 30, 2026

Ethyl Acetate → (R)-4-Phenylsulfanylmethyl-4,5-dihydro-oxazol-2-ylamine

https://huagongshe.com/reaction/1911540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-2-Amino-3-phenylsulfanyl-propan-1-olHCID 68714506—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(R)-4-Phenylsulfanylmethyl-4,5-dihydro-oxazol-2-ylamineHCID 59323832—

Reaction Steps

To a stirred mixture of (R)-2-amino-3-phenylsulfanyl-propan-1-ol (0.09 g, 0.49 mmol) and K2CO3 (0.081 g, 0.59 mmol) in THF (3 ml) under an argon atmosphere was added a solution of cyanogen bromide (0.062 g, 0.59 mmol) in THF (1 ml). The mixture was stirred overnight, then ethyl acetate and water were added. The aqueous phase was back-extracted with EtOAc. The combined organics were dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (column: Isolute® Flash-NH2 from Separtis; eluent: EtOAc/MeOH=95:5) to yield a light yellow solid, (0.026 g, 26%); MS (ISP): 209.1 ((M+H)+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-d9173c69c31444c49aa0270be65319d5
Source noteuspto-grants-2013_12