HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043404Generated: October 30, 2026
2,4-Dichlorophenol → HCID 56649063, compound
https://huagongshe.com/reaction/1043404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichlorophenol | HCID 8449 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorodichloridic acid, phenyl ester | HCID 13038 | — |
| Reactant | 39825-33-7 | HCID 13089460 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 56649063 | HCID 56649063 | 66% |
Reaction Steps
Phenyl phosphorodichloridate (10.0 g, 47.4 mmol) was dissolved in 60 mL of dry DCM and subsequently cooled to −78° C. Slow addition of a preformed mixture of 2,4-dichlorophenol (7.73 g, 47.4 mmol) and triethylamine (7.27 mL, 52.1 mmol) in 20 mL of DCM was followed by stirring at above temperature for 30 min. The reaction was brought to 0° C. and stirred for 2.5 h at this temperature before (L)-alanine isopropyl ester (7.95 g, 47.4 mmol) was added as a solid in one batch. Stirring for 40 min at 0° C. was then followed by addition of more triethylamine (13.9 mL, 99.54 mmol) and additional stirring for 3 h at 0° C. or until judged complete by TLC (ethyl acetate/hexane=1/3). The reaction mixture was subsequently evaporated under reduced pressure and finally submitted to column chromatography (ethyl acetate in hexane) on silica gel to yield the product (mixture of two isomers) in 66% yield (13.6 g) as a viscous colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08563530B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-9d11396abde641069246eb982963eabb |
|---|
| Source note | uspto-grants-2013_10 |
|---|