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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600839Generated: October 29, 2026

Hydrochloric Acid → HCID 57667120, compound

https://huagongshe.com/reaction/600839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 67272192HCID 67272192—
ProductHCID 57667120HCID 5766712071%

Reaction Steps

To a stirred solution of (S)-4-{[(4-benzyl-phenyl)-ethyl-amino]-methyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (405 mg; prepared in analogy to example 1.a and 1.b starting from tert-butyl (R)-(+)-4-formyl-2,2-dimethyl-3-oxazolinecarboxylate and 4-benzylaniline) at r.t. in dioxane (5 ml) under an argon atmosphere was added HCl solution (4M in dioxane; 4.77 ml). The mixture was stirred overnight 16 h, then concentrated. The residue was taken up in CH2Cl2/MeOH 95:5 and 1N NaOH. The aqueous phase was back extracted with CH2Cl2/MeOH 95:5. The combined organics were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (Isolute® SPE flash NH2 column, aminopropyl-functionalized silica; gradient:CH2Cl2->CH2Cl2/MeOH 9:1) to give (S)-2-amino-3-[(4-benzyl-phenyl)-isopropyl-amino]-propan-1-ol (192 mg, 71%) as colorless amorphous solid. MS (ISP): 285.3 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902238B2
Source datasetuspto-grants-2011_03
ORD IDord-b9ab6a5b0ad640e0adf39e6a2dbb8902
Source noteuspto-grants-2011_03