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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459724Generated: November 4, 2026

(3R)-1-(tert-Butoxycarbonyl)-3-[(4-fluorobenzylthio)methyl]pyrrolidine → (3R)-3-[(4-Fluorobenzylthio)methyl]pyrrolidine

https://huagongshe.com/reaction/1459724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R)-1-(tert-Butoxycarbonyl)-3-[(4-fluorobenzylthio)methyl]pyrrolidineHCID 54249072—
SolventFormic AcidHCID 284—
Product(3R)-3-[(4-Fluorobenzylthio)methyl]pyrrolidineHCID 54446756103.7%

Reaction Steps

A solution of (3R)-1-(tert-butoxycarbonyl)-3-[(4-fluorobenzylthio)methyl]pyrrolidine (0.5422 g, 1.67 mmol) in 90% formic acid (5 ml) was stirred at room temperature for 23 h. The solvents were removed in vacuo and the residue was dissolved in dichloromethane (25 ml) and washed with 2N NaOH solution (10 ml). The aqueous layer was reextracted with more dichloromethane (25 ml) and the combined organic extracts were washed with saturated NaCl solution (10 ml), dried (Na2SO4) and evaporated in vacuo to leave 0.3903 g of the title compound as an oil. δH (360 MHz, CDCl3) 1.42 (1H, m), 1.94 (1H, m), 2.24 (1H, m), 2.45 (2H, m), 2.59 (1H, m), 2.92 (2H, m), 3.08 (1H, m), 3.69 (2H, s), 7.00 (2H, t, J=8.6 Hz), 7.25-7.29 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854268
Source datasetuspto-grants-1998_12
ORD IDord-e49b673b92f442ee967e7f4ba6891cf9
Source noteuspto-grants-1998_12