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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416577Generated: October 25, 2026

2,4,5-Trichlorophenol → Cbz-D-hPro-Pro-OH

https://huagongshe.com/reaction/1416577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,5-TrichlorophenolHCID 7271—
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantL-ProlineHCID 145742—
Reactant(2R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acidHCID 688346—
SolventEthyl AcetateHCID 8857—
ProductCbz-D-hPro-Pro-OHHCID 22854903—

Reaction Conditions

Temperature0 °C

Reaction Steps

Cbz-D-hPro-OH (9.5 g, 36 mmol) was dissolved in ethyl acetate (100 mL) and the solution cooled to 0° C. Added to the solution was 2,4,5-trichlorophenol (7.1 g, 36 mmol) and 1,3-dicyclohexylcarbodiimide (7.4 g, 36 mmol). The reaction was stirred for 1 hour at 0° C. and 1 hour at room temperature. The precipitate was filtered and the filtrate concentrated in vacuo to an oil. The oil was dissolved in pyridine (100 mL), Pro-OH (4.2 g, 36 mmol), and triethylamine (5.0 mL, 36 mmol) were added. The reaction was stirred at room temperature (24 hours). The reaction solvent was removed in vacuo to an oil. The residue was dissolved in water (100 mL), diethyl ether (50 mL) was added and the pH adjusted to 9.5 with 2 N sodium hydroxide. The aqueous layer extracted twice with diethyl ether. The aqueous layer separated, the pH adjusted to 2.8 with 3 N hydrochloric acid and ethyl acetate (150 mL) was added. The organic layer was separated, dried (MgSO4), and the filtrate evaporated in vacuo to an amorphous solid (11.4 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05914319
Source datasetuspto-grants-1999_06
ORD IDord-fb97aaa6b5a3410b92e6af4e0e23de7c
Source noteuspto-grants-1999_06