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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601052Generated: November 1, 2026

O-Phenylenediamine → HCID 19591898, compound

https://huagongshe.com/reaction/1601052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantGlycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 19591898HCID 1959189870%

Reaction Steps

A solution of phenylenediamine (100 g, 0.924 mole) and Boc-sarcosine (175 g, 0.924 mole) in DMF (1750 mL) was cooled to -10° C. under argon, and a solution of DCC (190.8 g, 0.924 mole) in CH2Cl2 (1750 mL) was added in a slow stream over 1 hr. The temperature rose to 0° C. during the addition. The reaction was stirred overnight while the temperature was allowed to rise to RT. The white precipitate was removed by filtration, and the filtrate was diluted with H2O (3.5 L) and saturated brine (1 L). The CH2Cl2 layer was separated and the aqueous phase was extracted with EtOAc (2×1 L). The combined organic layers were washed with H2O (1 L) and brine (0.5 L), then were concentrated to a yellow residue (341 g). This was triturated with EtOAc to afford the title compound (179.4 g, 70%): mp 134-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977101
Source datasetuspto-grants-1999_11
ORD IDord-31d8437c65dd425eab40c4f7f188d207
Source noteuspto-grants-1999_11