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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276370Generated: October 30, 2026

Trifluoroacetic acid → HCID 66705887, compound

https://huagongshe.com/reaction/2276370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66705883HCID 66705883—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventSodium HydroxideHCID 14798—
ProductHCID 66705887HCID 66705887100.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of trifluoroacetic acid (0.07 ml) in water (6 ml) was added dropwise a solution of (S)-4-[(S)-2-(3-benzyloxy-phenoxy)-butyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (135 mg) in acetonitrile (1 ml). The mixture was heated for 4 h at 80° C. with mechanical shaking. The mixture was then cooled to room temperature and diluted with 1 N aqueous sodium hydroxide solution. The mixture was extracted twice with ethyl acetate and the combined organic phases were dried over sodium sulphate and concentrated in vacuo to give (2S,4S)-2-amino-4-(3-benzyloxy-phenoxy)-hexan-1-ol (94 mg, quant.) as a light yellow viscous oil. MS (ISP): 316.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132136B2
Source datasetuspto-grants-2015_09
ORD IDord-0f1cb4485dc24b86bd64bdf94d117e17
Source noteuspto-grants-2015_09