Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407366Generated: October 29, 2026

Triethylamine → HCID 59226759, compound

https://huagongshe.com/reaction/2407366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIdramantoneHCID 64184—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantAmmonium formateHCID 2723923—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59226759HCID 5922675997%

Reaction Conditions

Temperature20 °C

Reaction Steps

Ammonium formate (10 g, 0.15 mol) was added to a solution of 5-hydroxyadamantan-2-one (4.5 g, 0.027 mol, prepared as described in Tetrahedron 1968, 24, 5369) in MeOH (50 ml). Then 10% Pd—C (500 mg) was added carefully and the solution heated under reflux for 1 h. It was then filtered through celite and to this filtrate at 0° C. was added triethylamine (11.2 ml, 0.081 mol) and Boc anhydride (7.06 g, 0.0324 mol). The solution was stirred for 4 h at 20° C. and then concentrated under reduced pressure. The residue was diluted with water and extracted with EtOAc. The organic layer was dried and concentrated to give (5-hydroxyadamantan-2-yl)carbamic acid tert-butyl ester (7 g, 96%). LC-MS (m/z): 168 (M+1). 1H NMR (300 MHz, DMSO-d6): δ 6.8 (d, 1H), 6.7 (brs, 1H), 3.45 (d, 1H), 2.0 (s, 1H), 1.75-1.95 (m, 4H), 1.5-1.7 (m, 6H), 1.35 (s, 9H), 1.25 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809540B2
Source datasetuspto-grants-2014_08
ORD IDord-61c4d0e2fa1e4832a31374bd17885730
Source noteuspto-grants-2014_08