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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734654Generated: October 31, 2026

Isopropyl iodide → HCID 57845587, compound

https://huagongshe.com/reaction/734654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 24804916HCID 24804916—
SolventAcetoneHCID 180—
ProductHCID 57845587HCID 5784558783.4%

Reaction Steps

1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU, 5.4 μL, 0.036 mmol) and 2-iodopropane (48 μL, 0.48 mmol) were added to a solution of acid 11c (11 mg, 0.024 mmol) in acetone (0.3 mL) at room temperature under nitrogen. After 3 days at room temperature, the reaction mixture was concentrated in vacuo. The residue was acidified with 1.0 N HCl (5 mL) extracted with EtOAc (10 mL). The organic phase was washed with brine (5 mL), dried (MgSO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on 3 g silica (10% MeOH/CH2Cl2, gradient) afforded 10 mg (83%) of the title compound (18). 1H NMR (500 MHz, CDCl3) δ□ppm 1.21-1.32 (m, 6 H), 1.32 (s, 3 H), 1.34 (s, 3 H), 1.75-1.80 (m, 6 H), 2.62 (ddd, J=13.91, 9.69, 6.72 Hz, 1 H), 2.71 (td, J=9.35, 5.01 Hz, 1 H), 2.84 (t, J=7.40 Hz, 2 H), 4.03 (q, J=7.09 Hz, 1 H), 4.08-4.18 (m, 1 H), 4.65 (s, 2 H), 5.17 (dt, J=12.47, 6.24 Hz, 1 H), 6.77 (d, J=3.67 Hz, 1 H), 7.08 (d, J=9.54 Hz, 2 H), 7.18 (s, 1 H), 7.60 (d, J=3.67 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592366B2
Source datasetuspto-grants-2009_09
ORD IDord-5c641067bb8642e999e108153486ffef
Source noteuspto-grants-2009_09