HCID 22914116, compound → HCID 22914108, compound
Reaction equation
[CH3:1][C:2]1([CH3:16])[CH2:6][CH:5]([CH:7]2[CH2:11][CH:10]=[C:9]([CH3:12])[C:8]2([CH3:14])[CH3:13])[CH:4]([CH3:15])[O:3]1>[Pd]>[CH3:1][C:2]1([CH3:16])[CH2:6][CH:5]([CH:7]2[CH2:11][CH2:10][CH:9]([CH3:12])[C:8]2([CH3:14])[CH3:13])[CH:4]([CH3:15])[O:3]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The tetrahydrofuran mixture from Example 13, 35.5 g at 96.7% (0.154 mole) was hydrogenated at 60 psi at 40-50° C. using 0.75 g of 5% Pd on carbon. The crude product, 35.7 g, was distilled to yield 34.4 g of purified product (100% yield). BP 53° C./0.04 mmHg; 1H-NMR (300 MHz), spectra consistent with assigned structures. 13C-NMR (75 MHz), spectra consistent with assigned structures. IR (Neat), 2990, 1490, 1130, 1110 cm-1 ; MS (m/e), 209 (M+ -15), 110, 96 (Base);
Workup
- customwas hydrogenated at 60 psi at 40-50° C.
- distillationThe crude product, 35.7 g, was distilled
Sources & evidence
- ORD record
- ord-3f0cac48d2054993864a7e3fb8984213
- Source dataset
- uspto-grants-1997_09
- Patent number
- US05665696
Reaction notes
Loading…