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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944196Generated: October 30, 2026

Hydrazine hydrate (1:1) → HCID 12275569, compound

https://huagongshe.com/reaction/1944196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 68497223HCID 68497223—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 12275569HCID 1227556976%

Reaction Conditions

Temperature40 °C

Reaction Steps

Raney nickel (50%, slurry in water, 2.0 g) was washed with MeOH (3×). To this was added MeOH (70 ml) and 209 (3.05 g, 10.1 mmol). The mixture was cooled (ice-bath) and hydrazine hydrate (2.53 g, 50.5 mmol) was added dropwise. The mixture was heated to 40° C. for 1 h, then further Raney nickel (50% slurry in water, 1.0 g) was added as a suspension in MeOH (10 ml). The reaction mixture was heated at 40° C. for a further 18 h. The resulting solution was cooled to rt and filtered through celite, washing through with MeOH (200 ml). The filtrate was concentrated in vacuo and purification (flashmaster: 50 g, EtOAc/MeOH) afforded the title compound (2.074 g, 76%) as a pale yellow oil. 1H NMR (270 MHz; CDCl3) 1.04 (3H, d, J=6.4 Hz, CH3), 2.36 (1H, dd, J=13.3, 8.2 Hz, CHH), 2.58 (1H, dd, J=13.3, 5.2 Hz, CHH), 2.98-3.1 (1H, m, CH), 3.86 (3H, s, OCH3), 5.13 (2H, s, CH2), 6.67-6.83 (3H, m, 3×CH), 7.25-7.43 (5H, m, 5×CH, phenyl). LC/MS (ES+) tr=1.82 min, m/z 272.19 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394825B2
Source datasetuspto-grants-2013_03
ORD IDord-9a219029df064f09a28a85185c380505
Source noteuspto-grants-2013_03