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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809789Generated: November 2, 2026

Tetrahydrofuran → HCID 67542919, compound

https://huagongshe.com/reaction/1809789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 19705303HCID 19705303—
SolventWaterHCID 962—
ProductHCID 67542919HCID 67542919—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a stirred mixture of the title A compound, 4-biphenyl-3-yl-3,6,dihydro-2H-pyridine-1-carboxylic acid t-butyl ester (2.57 g, 7.66 mmol) and 6 mL of dry THF is added dropwise under argon at 5° C. a 1M borane-tetrahydrofuran complex solution (11 mL, 11 mmol) within 15 min. The reaction mixture is stirred for 10 min. at 5° C. and for 1 h at RT. NaBO3 (3.38 g, 22 mmol) is then added in several portions followed by H2O (10 mL). After 2 h at RT, the reaction mixture is extracted twice with ethyl acetate. The combined organic extracts are dried (Na2SO4) and evaporated in vacuo. Flash chromatography of the residue (SiO2, hexane/ethyl acetate) affords (3R*,4R*)-4-biphenyl-3-yl-3-hydroxy-piperidine-1-carboxylic acid t-butyl ester as a white amorphous solid: MS (after treatment with trifluoroacetic acid) 254.3 [M+H—C5H8O2]+; Rf 0.10 (hexane/ethyl acetate 8:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362040B2
Source datasetuspto-grants-2013_01
ORD IDord-e4345caf6b194b0ab9edf1cf4ed97e5c
Source noteuspto-grants-2013_01