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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015513Generated: October 30, 2026

HCID 86761366, compound → HCID 86761367, compound

https://huagongshe.com/reaction/1015513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86761366HCID 86761366—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86761367HCID 8676136795%

Reaction Steps

To a stirred mixture of tert-butyl [1-(benzyloxymethyl)tricyclo[3.3.1.03,7]non-3-yl]carbamate (1.0 g, 2.8 mmol) obtained in step V in MeOH (11 mL), Pd/C (10%, 0.2 g) was added. The H2 pressure was then applied with the balloon for 2 h. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated under reduced pressure to obtain tert-butyl [1-(hydroxymethyl)tricyclo[3.3.1.03,7]non-3-yl]carbamate as a viscous liquid (0.7 g) in 95% yield. m/z (M+1) 268; 1H NMR (CDCl3) 300 MHz δ 4.74 (s (br), 1H), 3.45 (s, 2H), 2.50-2.40 (m, 1H), 2.40-2.33 (m, 1H), 2.05-1.87 (m, 4H), 1.80 (dd, J=2.4, 10.3 Hz, 1H), 1.65 (dd, J=3.0, 10.0 Hz, 1H), 1.54-1.40 (m, 3H), 1.45 (s, 9H), 1.37 (dd, J=3.1, 10.0 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985759B2
Source datasetuspto-grants-2011_07
ORD IDord-0ddc59525c284f80a492af9d29c30b63
Source noteuspto-grants-2011_07