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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859883Generated: October 30, 2026

Sodium Chloride → (3R,4R)-3-azidomethyl-1-benzyloxycarbonyl-4-hydroxypyrrolidine

https://huagongshe.com/reaction/859883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(3R,4R)-3-Azidomethyl-1-benzyloxycarbonyl-4-(tert-butyldimethylsilyl)oxypyrrolidineHCID 86600233—
SolventTetrahydrofuranHCID 8028—
Product(3R,4R)-3-azidomethyl-1-benzyloxycarbonyl-4-hydroxypyrrolidineHCID 8660023293.2%

Reaction Steps

(3R,4R)-3-Azidomethyl-1-benzyloxycarbonyl-4-(tert-butyldimethylsilyl)oxypyrrolidine (3.05 g) was dissolved in tetrahydrofuran (50 mL). While this solution was cooled on an ice bath, tetrabutylammonium fluoride (lmol/L tetrahydrofuran solution, 13.3 mL) was added dropwise and the mixture was stirred for additional 1 hour. Subsequently, a saturated aqueous solution of sodium chloride 70 mL) was added and the mixture was extracted with ethyl acetate (150 mL, 100 mL). The ethyl acetate extracts were combined and the combined solvent was dried over anhydrous sodium sulfate and was concentrated under reduced pressure. The resulting residue was purified on a silica gel column (eluant=ethyl acetate) to give 2.01 g of (3R,4R)-3-azidomethyl-1-benzyloxycarbonyl-4-hydroxypyrrolidine as a milky white syrup-like product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153851B2
Source datasetuspto-grants-2006_12
ORD IDord-a36ca6eb86fa417aa83366291412673c
Source noteuspto-grants-2006_12