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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386955Generated: November 1, 2026

Dichloromethane → HCID 86757201, compound

https://huagongshe.com/reaction/1386955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantN-benzyl-3-pyrrolidinolHCID 69889—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178464503HCID 178464503—
ProductHCID 86757201HCID 8675720153%

Reaction Steps

To a solution of (RS)-N-benzyl-3-pyrrolidinol (354 mg, 2.0 mmol) in CH2Cl2 (6 ml) was added diethylaminosulfur tetrafluoride (DAST) (0, 52 ml, 4.0 mmol) over 5 min. at 0-5° C. The mixture was stirred for a further 1.5 hrs. at r.t., then satd. NaHCO3 was added and the oragnic phase was further washed with NaHCO3 (10 ml). After drying the organic phase with Na2SO4 the residue was chromatographed over SiO2 (Merck 230-400 mesh) with nhexane/EtOAc (4:1) gradient to (1:1). The product was treated with HCl/ether to afford (RS)N-benzy-3-fluoropyrrolidine hydrochloride salt (190 mg, 1.06 mmol, 53% yield) as off-white crystals. This product (250 mg, 1.16 mmol) was then hydrogenated (1 atm. H2) in acetic acid (4 ml) at 100° C. with Pd/C (10%, 25 mg) for 24 hrs. The mixture was then evaporated and dissolved in MeOH, filtered though a celite pad and finally recrystallised from EtOAc/ether to afford the title compound (117 mg, 81% yield) as off-white crystals after drying under high vacuum. MS: m/e=89 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265426B1
Source datasetuspto-grants-2001_07
ORD IDord-614e295525c345099140ba10e3f02c74
Source noteuspto-grants-2001_07