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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626538Generated: October 30, 2026

1,2-Dichloroethane → 4-methyltetrahydro-2H-pyran-4-carboxamide

https://huagongshe.com/reaction/626538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-METHYLTETRAHYDRO-2H-PYRAN-4-CARBOXYLIC ACIDHCID 11571820—
CatalystAmmonium HydroxideHCID 14923—
SolventAcetonitrileHCID 6342—
Product4-methyltetrahydro-2H-pyran-4-carboxamideHCID 5791151471%

Reaction Steps

A mixture of 4-methyltetrahydro-2H-pyran-4-carboxylic acid (2.60 g, 18.0 mmol), HOBt (2.76 g, 18.0 mmol) and EDC (4.49 g, 23.4 mmol) in MeCN (75 mL) was stirred at RT for 3 h, treated with NH4OH (˜15M, 7 mL, −105 mmol) and stirred at RT overnight. The mixture was concentrated to dryness, and the residue was partitioned between satd. Brine (40 mL) and DCM (100 mL). The aqueous was extracted with THF (50 mL) and DCM (5×30 mL). The combined organics were washed with 10% aq K2CO3 (50 mL), dried over Na2SO4 and concentrated in vacuo to afford 4-methyltetrahydro-2H-pyran-4-carboxamide (1.83 g, 70%). 1H NMR (400 MHz, DMSO-d6): δ 7.14 (s, 1H), 6.86 (s, 1H), 3.60 (dt, J=11.7, 4.5 Hz, 2H), 3.36 (m, 2H), 1.91-1.89 (m, 2H), 1.30 (m, 2H), 1.08 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309224B2
Source datasetuspto-grants-2016_04
ORD IDord-0ca184cb7e384408b7bb30321c0322a6
Source noteuspto-grants-2016_04