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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592979Generated: October 30, 2026

Trifluoroacetic acid → HCID 86610938, compound

https://huagongshe.com/reaction/1592979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl AcetateHCID 8857—
ReactantTriethylsilaneHCID 12052—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86598940HCID 86598940—
ProductHCID 86610938HCID 86610938100%

Reaction Steps

21 g (47.3 mmol) of methyl (2S,3R)-3-{3′-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yl}-2-ethoxy-3-hydroxypropionate, 8.76 ml (54.9 mmol) of triethylsilane in 300 ml of trifluoroacetic acid are introduced into a round-bottomed flask and under a nitrogen stream. The reaction medium is stirred for 4 hours at room temperature. Ethyl acetate is then added and the mixture is neutralized with sodium hydroxide. The organic phase is washed with a saturated aqueous sodium chloride solution, dried over magnesium sulphate, filtered and evaporated off. 19.6 g (100%) of the expected crude product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294639B2
Source datasetuspto-grants-2007_11
ORD IDord-6e5dd99a3f8f45f085e53a7275b4e4de
Source noteuspto-grants-2007_11