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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922472Generated: October 30, 2026

Tris(1,1-dimethylethyl)phosphine → HCID 59807032, compound

https://huagongshe.com/reaction/1922472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-Butyl 4-(5-bromo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylateHCID 22029161—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59807032HCID 59807032104.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of Pd2(dba)3 (0.08 g, 0.087 mmol) in dry THF (5 mL) was treated with PtBu3 (1.06 mL, 0.351 mmol, 10% in hexanes), followed by compound 3 (0.67 g, 1.757 mmol) in dry THF (5 mL) and LiHMDS (3.51 mL, 3.514 mmol) at room temperature. The resulting mixture was stirred at 100° C. in a seal tube for 3 h. The reaction was brought to room temperature and quenched with TBAF (5 mL, 1 M solution in THF). After stirring for 15 min., solution was basified with 1 N NaOH solution (50 mL) and product was extracted into CH2Cl2 (3×20 mL). The combined CH2Cl2 layer was dried (Na2SO4) and evaporated to obtain the crude product. The crude was purified by column chromatography (2 M NH3 in MeOH:CH2Cl2, 2.5:97.5) to obtain compound 4 (0.4 g, 72%) as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173813B2
Source datasetuspto-grants-2012_05
ORD IDord-3defb879195d4271a53df15df698a88b
Source noteuspto-grants-2012_05