HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976946Generated: October 31, 2026
2,6-Dichlorobenzoyl chloride → (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester
https://huagongshe.com/reaction/1976946
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dichlorobenzoyl chloride | HCID 78392 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Amino-N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl ester | HCID 11011855 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester | HCID 54393861 | 100.3% |
Reaction Steps
To a solution of 4-amino-N-[(1,1-dimethylethoxyl)carbonyl]-L-phenylalanine methyl ester 2.6 g, 8.6 mmol) in dichloromethane (20 mL) were added diisopropylethylamine (2.3 mL, 13 mmol) followed by 2,6-dichlorobenzoyl chloride (1.99 g, 9.5 mmol) at room temperature. The mixture was stirred for 15 hr at which time a white precipitate formed. The mixture was diluted with 30 mL of dichloromethane and 50 mL of water. The layers were separated and the aqueous layer was extracted with dichloromethane (2×50 mL). The combined extracts were washed with brine and dried over anhydrous magnesium sulfate. Filtration and concentration of the solvent gave 4.03 g (quant) of 4-[(2,6-dichlorophenylcarbonyl)amino]-N-[(1,1-dimethylethoxyl)carbonyl]-L-phenylalanine methyl ester as a white solid: mp 148-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06229011B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-99ef85d0e1e44c8a8b5d7b071d86be03 |
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| Source note | uspto-grants-2001_05 |
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