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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808656Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 86603903, compound

https://huagongshe.com/reaction/1808656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantSodium HydroxideHCID 14798—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantEthyl acetohydroximateHCID 99894—
Reactant8-Bromooctanoic acidHCID 548275—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86603903HCID 8660390334%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of ethyl N-hydroxyacetimidate 1 (6.2 g, 60 mmol) and 8-bromooctanoic acid (15 g, 67 mmol) in 150 mL of solvent mixture (methanol 8:acetone 1) was added drop wise 22 mL of 10N NaOH and heated at 50° C. for 12 h. The reaction mixture was cooled, the organic solvent was removed by rotary evaporation. The dilute HCl solution was added to adjust pH down to 6. The resulting turbid mixture was extracted with CHCl3 and EtOAc. The extract was washed with brine, dried, filtered, and solvent was evaporated to crude oil (3, 12 g, 49 mmol, 82%). A mixture of 3 (12 g, 49 mmol) and N-hydroxysuccinimide (5 g, 50 mmol) in 100 mL of THF was treated with 50 mL of DCC (1.0M solution in CH2Cl2). The solids were filtered, and the clear filtrate was evaporated. The resultant brown oil was purified on a silica gel column. Elution with 20% ethyl acetate/hexane afforded 5.8 g (17 mmol, 34%) of the product as a wet solid. 1H NMR (DMSO-d6): δ 1.21 (3H, t, J=7.0), 1.28-1.38 (6H, m), 1.57 (2H, p, J=6.8), 1.64 (2H, p, J=7.4), 1.86 (3H, s), 2.65 (2H, t, J=7.5), 2.81 (4H, s), 3.82 (2H, t, J=6.5), 3.94 (2H, q, J=7.0)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361442B2
Source datasetuspto-grants-2013_01
ORD IDord-856dea325a954c25a728ddc45c1ef343
Source noteuspto-grants-2013_01