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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922641Generated: October 30, 2026

HCID 59605965, compound → HCID 59605642, compound

https://huagongshe.com/reaction/1922641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59605965HCID 59605965—
CatalystPalladiumHCID 23938—
ProductHCID 59605642HCID 5960564292.2%

Reaction Steps

A mixture of 3-(3,6-dihydro-2H-pyran-4-yl)azetidine-1-carboxylic acid tert-butyl ester (28.6 g, 0.12 mol) and 10% palladium on charcoal (5.0 g) in IMS (500 mL) was stirred under hydrogen (4 bar) at room temperature for 36 hours. The reaction mixture was filtered through a bed of Celite® which was washed with IMS. The filtrates were combined and concentrated to give a residue which was reacted as above for 18 hours. The reaction mixture was worked up as above to give a residue which was dried under reduced pressure to give 3-(Tetrahydropyran-4-yl)azetidine-1-carboxylic acid tert-butyl ester as a beige solid (26.7 g, 92%). 1H NMR (300 MHz, CHCl-d): δ 4.03-3.90 (m, 4H); 3.63 (dd, J=8.6, 5.7 Hz, 2H); 3.37 (td, J=11.8, 2.0 Hz, 2H); 2.32-2.19 (m, 1H); 1.63-1.48 (m, 3H); 1.44 (s, 9H); 1.29-1.12 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173650B2
Source datasetuspto-grants-2012_05
ORD IDord-f80476cf451b4a5f913be244e477898c
Source noteuspto-grants-2012_05