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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214256Generated: October 26, 2026

Diisopropylcarbodiimide → HCID 131725937, compound

https://huagongshe.com/reaction/2214256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-(triphenylmethyl)hydroxylamineHCID 3015602—
Reactant3-Methoxycarbonyl-hexanedioic acid 1-tert-butyl esterHCID 86594384—
SolventDimethylformamideHCID 6228—
ProductHCID 131725937HCID 131725937—

Reaction Steps

To a solution of the compound of example 64 (1.10 g, 4.19 mmol) and HOBt (0.70 g, 5.03 mmol) in DMF (5 mL) were added O-trityl hydroxylamine (1.82 g, 6.28 mmol) and DIC (800 μL), respectively. The reaction mixture was stirred for 24 h at room temperature. The reaction mixture was partitioned between HCl (1N, excess) and ethyl acetate. The aqueous phase was extracted several times with ethyl acetate. The recombined organic layer was washed with brine, saturated sodium bicarbonate, and brine. The solvent was evaporated following drying over sodium sulfate, and the crude was flashed with 20–30% ethyl acetate in hexanes. 1H-NMR(CDCl3, 400 MH: 1.42(s, 9H); 1.58, 2.14, 2.47(3 m, 7H); 3.69(s, 3H); 7.34(m, 15H); 7.88(d, broad, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105539B2
Source datasetuspto-grants-2006_09
ORD IDord-ba55ca6f587b46729aa9409d8a9a32c0
Source noteuspto-grants-2006_09