Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453651Generated: November 1, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 69058421, compound

https://huagongshe.com/reaction/1453651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 22324258HCID 22324258—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventDiethyl EtherHCID 3283—
SolventO-XyleneHCID 7237—
ProductHCID 69058421HCID 6905842197.3%

Reaction Steps

A mixture of 0.5 g (1.51 mmole) 1-(3-bromo-benzyl)-1,3,4,5-tetrahydro-benzo[b]azepin-2-one, 0.203 g sodium tert-butoxide, 0.04 g (0.16 mmole) tri-tert-butyl phosphine, 0.04 g (0.16 mmole) palladium(II)acetate, and 0.3 g piperazin-1-yl carboxylic acid tert-butyl ester in 5 mL xylene was heated at 105° under N2 for 1.5 hrs. The mixture was diluted with 5 mL ethyl ether and then filtered through a pad of 10 g silica gel 230-400 mesh. 4-[3-(2-Oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-ylmethyl)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester was eluted with 20% ethyl acetate/hexane to yield 0.64 g of a heavy syrup. M+H=436.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476675B2
Source datasetuspto-grants-2009_01
ORD IDord-0b4183f0a8de47a19b7a15fd6c782b7f
Source noteuspto-grants-2009_01