Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915819Generated: November 2, 2026

Trimethylphosphine → HCID 86680028, compound

https://huagongshe.com/reaction/1915819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylphosphineHCID 68983—
ReactantHCID 86680026HCID 86680026—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86680028HCID 8668002889%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 5-azido-1-benzyl-5-methylazepan-4-ol (1.5 g, 5.76 mmol) in THF (12 mL) and water (4 mL) was added slowly a solution of trimethylphosphine (1 M in toluene, 28 mL, 28.9 mmol) and the reaction was stirred at 65° C. for 18 hr. The mixture was allowed to cool to room temperature and concentrated under reduced pressure. The residue was dissolved in 1 M HCl (30 mL) and extracted with EtOAc (2×25 mL). The aqueous layer was basified to pH14 with aqueous 6 M NaOH and extracted with DCM (3×30 mL). The combined organic layers were passed through a phase separation cartridge concentrated under reduced pressure. Purification via silica gel column chromatography (1-10% 7 M NH3 in MeOH/DCM) gave 5-amino-1-benzyl-5-methylazepan-4-ol as a viscous yellow oil (1.2 g, 89%). 1H NMR (400 MHz, CDCl3) δ 7.34-7.20 (m, 5H), 3.60-3.52 (m, 2H), 3.50-3.46 (m, 2H), 2.80-2.79 (m, 1H), 2.70-2.45 (m, 4H), 2.15-1.95 (m, 1H), 1.79-1.72 (m, 2H), 1.49-1.40 (m, 2H), 1.19 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614206B2
Source datasetuspto-grants-2013_12
ORD IDord-a7b33c9561534db8902a2a2850ce675f
Source noteuspto-grants-2013_12