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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698890Generated: November 2, 2026

Allyl Alcohol → HCID 18322378, compound

https://huagongshe.com/reaction/1698890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 2757206HCID 2757206—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 18322378HCID 1832237866%

Reaction Steps

To a solution of 3-(N-carbo-tert-butoxyamino)-5-tert-butylthiophene-2-carboxylic acid (0.20 g, 0.67 mmol), allyl alcohol (0.042 g, 0.73 mmol, 1.1 equiv) and DMAP (0.008 g, 0.07 mmol, 10 mol %) in CH2Cl2 (2 mL) was added EDCI.HCl (0.14 g, 0.73 mmol, 1.1 equiv). The CH2Cl2 mixture was stirred at room temp. for 3 d, diluted with CH2Cl2, washed with a 1N HCl solution (5 mL) and a saturated NaHCO3 solution (5 mL), dried (Na2SO4), and concentrated under reduced pressure to afford allyl 3-(N-carbo-tert-butoxyamino)-5-tert-butylthiophene-2-carboxylate (0.15 g, 65%) as a colorless oil: TLC (50% CH2Cl2/hexane) Rf0.63; 1H NMR (CDCl3) δ1.37 (s, 9H), 1.50 (s, 9H), 4.74 (ddd, J=5.5, 1.5, 1.5 Hz, 2H), 5.26 (dd, J=10.3, 1.5 Hz, 1H), 5.37 (dd, J=17.3, 1.5 Hz, 1H), 5.87-5.98 (m, 1H), 7.68, 9.35; 13C NMR (CDCl3) δ28.2 (3C), 31.8 (3C), 35.2, 64.9, 80.8, 104.9, 116.4, 118.1, 132.0, 145.6, 152.1, 164.0, 164.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344476B1
Source datasetuspto-grants-2002_02
ORD IDord-2618625a33da4f3597ff8398c83c008a
Source noteuspto-grants-2002_02