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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354112Generated: November 1, 2026

Water → HCID 68502963, compound

https://huagongshe.com/reaction/2354112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTetrahydrofuran heptaneHCID 21263495—
ReactantHCID 25178693HCID 25178693—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68502963HCID 6850296379%

Reaction Steps

To a solution of trans-2-bromo-5′-chloro-2′-hydroxystilbene (81 g, 261 mmol) in tetrahydrofuran (570 ml) trimethylamine-N-oxide.dihydrate (43.4 g, 390 mmol) was added at ambient temperature. Lithium diisopropylamide in heptane/THF (2M, 1070 ml, 2140 mmol) was then added during the course of 1 hour while maintaining the temperature below 40° C. After completion of the reaction water (120 ml) was added. Solvent was evaporated to a small volume after which ethyl acetate (250 ml) was added. The pH was adjusted to pH 8 with 18 % hydrochloric acid (˜250 ml) and ethyl acetate (250 ml) was added. The organic layer was separated and the aqueous layer was again extracted with ethyl acetate (2×120 ml). The combined organic layers were washed with water (325 ml) and with brine, dried (MgSO4) and then evaporated in vacuo. The resulting oil was crystallised from ethanol/water (1/1, v/v) to give the title pyrrolidine (62.0 g, 79%). Purity according to HPLC is 99% a/a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750167B2
Source datasetuspto-grants-2010_07
ORD IDord-9dbe5d24ebd24e8282f9bc22d507ab00
Source noteuspto-grants-2010_07