HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24693Generated: October 29, 2026
Potassium Carbonate → HCID 53892462, compound
https://huagongshe.com/reaction/24693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dimethoxy-4-(tert-butyl-diphenylsilyloxy)benzeneboronic acid | HCID 22571857 | — |
| Reactant | (S)-Ethyl 3-(4-bromophenyl)-2-(2,6-dichlorobenzamido)propanoate | HCID 54106344 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Product | HCID 53892462 | HCID 53892462 | 53.7% |
Reaction Steps
A mixture of 2,6-dimethoxy-4-(tert-butyl-diphenylsilyloxy)benzeneboronic acid (3 g), N-(2,6-dichlorobenzoyl)-4-bromo-L-phenylalanine ethyl ester (0.8 g), Pd(PPh3)4 (1 g) and K2CO3 (2.1 g) in DME/H2O (20 mL/0.5 mL) was heated at 80° C. for 6 hour under N2. The mixture was diluted with EtOAc and washed with water, dried and evaporated. The residue was dissolved in EtOAc and the solution was filtered through a silica gel column and evaporated. The residue was dissolved in THF, and TBAF (1.6 M in THF, 4 ml) was added. The mixture was stirred at room temperature for 1 hour, diluted with water and extracted with EtOAc. The extract was washed with water, dried and evaporated. The residue was purified by flash column chromatography (silica gel; eluent: EtOAc/hexane 1/2) to yield 0.5 g of N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxy-4-hydroxyphenyl)-L-phenylalanine ethyl ester. ESMS m/z: 490 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06855843B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-410ad7b90dea4035828019e4f37d1412 |
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| Source note | uspto-grants-2005_02 |
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