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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454339Generated: November 2, 2026

HCID 131727245, compound → HCID 85850727, compound

https://huagongshe.com/reaction/1454339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131727245HCID 131727245—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 85850727HCID 85850727—

Reaction Steps

A solution of 1.78 g (5.5 mmol) of (R/S)-1-tert-butoxycarbonyl-3-hydroxy-pyrrolidin-3-yl phosphonic acid, diethyl ester (from Step C) in 2N HCl in EtOH was stirred at rt for 5.5 h. The reaction was concentrated from CH2Cl2 several times. The crude product was partitioned between aqueous NH4OH and CHCl3/isopropanol (3:1 v/v). After separating phases, the aqueous layer was extracted with 3× CHCl3/isopropanol (3:1 v/v). The combined organics were dried over Na2SO4 and concentrated. The residue was purified on a 40S Biotage column using 90:10:1 v/v/v CH2Cl2/MeOH/NH4OH as the eluant to afford the title compound as a light brown oil: 1H-NMR (500 MHz) δ 1.35 (t, J=7.0, 6H), 1.92 (m, 1H), 2.20 (m, 1H), 2.78-2.99 (m, 3H), 3.06 (dd, J=12.7, 3.7, 1H), 3.13 (dd, J=12.7, 6.2, 1H), 3.20 (m, 1H), 4.16-4.23 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07479504B2
Source datasetuspto-grants-2009_01
ORD IDord-d001842697934d619ddd3364e27c8ed2
Source noteuspto-grants-2009_01