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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | tert-Butyl 4-(5-bromo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylate | HCID 22029161 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59807032 | HCID 59807032 | 104.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173813B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-3defb879195d4271a53df15df698a88b |
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| Source note | uspto-grants-2012_05 |
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