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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353438Generated: October 30, 2026

Diethylamine → HCID 10503756, compound

https://huagongshe.com/reaction/353438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 10834544HCID 10834544—
SolventDichloromethaneHCID 6344—
ProductHCID 10503756HCID 1050375673%

Reaction Steps

To a solution of compound 5 (1.0 g, 2.5 mmol) in dry dichloromethane (10 mL) at −20° C. was added isobutylchloroformate (450 mg, 3.3 mmol). After 20 min at −20° C. diethylamine (4 mL) was added and the reaction was allowed to warm to room temperature. After 1.5 hrs the solvents were evaporated and the residue was partitioned between ethyl acetate and water. The organic phase was washed with brine and dried over MgSO4. Removal of solvents provided a crude product, which was purified by flash chromatography to give compound 6 as white needles (800 mg, 73%): IR (NaCl) 3051, 2975, 1694, 1633, 1416, 1281, 1168, 1115 cm−1; 1H NMR (CDCl3) δ1.13 (br, 3H), 1.22 (br, 3H), 1.44 (s, 9H),2.22 (t, J=5.5 Hz, 2H), 2.62 (t, J=5.5 Hz, 2H), 3.33 (m, 4H), 3.55 (m, 2H), 7.31 (d, J=8.0 Hz, 2H), 7.36 (d, J=8.0 Hz, 2H); 13C NMR (CDCl3) δ12.71, 14.13, 28.3, 31.5, 34.2, 39.1, 43.2, 79.7, 115.9, 126.3, 129.3, 136.8, 137.1, 140.6, 154.6, 170.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753335B2
Source datasetuspto-grants-2004_06
ORD IDord-6557d14af52344c5bbc22dc4abf27f52
Source noteuspto-grants-2004_06