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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033951Generated: November 1, 2026

Trifluoroacetic acid → HCID 11132119, compound

https://huagongshe.com/reaction/1033951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86747094HCID 86747094—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11132119HCID 11132119—

Reaction Steps

To 186.3 g (4.9 mol) of sodium borohydride in 4 L of tetrahydrofuran (THF) was added (over a 30 minute period) 376 mL (4.9 mol) of trifluoroacetic acid (TFA), with ice water cooling to maintain temperature below 15° C. [2R,3S]-2,3-bis(((1,1-Dimethylethyl)dimethylsilyl)oxymethyl) cyclobutanone-O-methyl oxime (400 g, 1.03 mol), from Step 1E, in 3 L of THF was added with ice water cooling to maintain the temperature below 20° C. After stirring the reaction mixture at ambient temperature overnight, it was concentrated, diluted with methylene chloride (3 L) and washed portionwise (with cooling) with 400 mL of brine. After filtration, the layers of the filtrate were separated and the aqueous layer was washed with methylene chloride. The combined methylene chloride solution was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to give crude title compound which was taken on to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312963
Source datasetuspto-grants-1994_05
ORD IDord-dc29d8ebecb74ff3b7a0e29a65ed2654
Source noteuspto-grants-1994_05