HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475356Generated: October 31, 2026
O-Cresol → 3,3-Dimethyl-6-o-tolyloxy-2,3-dihydro-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1475356
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Cresol | HCID 335 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | tert-Butyl 6-chloro-3,3-dimethyl-2,3-dihydro-1H-pyrrolo[3,2-c]pyridine-1-carboxylate | HCID 86723969 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Di-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphane | HCID 11618717 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,3-Dimethyl-6-o-tolyloxy-2,3-dihydro-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester | HCID 86723971 | 71.7% |
Reaction Steps
A vessel containing 6-chloro-3,3-dimethyl-2,3-dihydro-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester (100 mg, 0.35 mmol), 2-methyl-phenol (38 mg, 0.42 mmol), 2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl (tBuXPhos) (5 mg, 0.01 mmol), Pd(OAc)2 (1.6 mg, 0.007 mmol) and potassium phosphate (150 mg, 0.70 mmol) in toluene (2 mL) was evacuated and flushed with nitrogen. The mixture was stirred at 110° C. overnight then were allowed to cool and then partitioned between EtOAc and water. The organic extract was washed with brine, dried (Na2SO4) and evaporated in vacuo. Chromatography (SiO2; gradient elution with 0-10% EtOAc in petrol) gave title compound (89 mg) {MS: [M+H]+=355} as an inseparable mixture with starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018214B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-cfd5ecabf56a4b27a4b5f50465876b31 |
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| Source note | uspto-grants-2015_04 |
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