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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049285Generated: October 31, 2026

1,2-Dichloroethane → Oxane-4-carboxamide

https://huagongshe.com/reaction/1049285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSodium ChlorideHCID 5234—
ReactantAmmonium HydroxideHCID 14923—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantOxane-4-carboxylic acidHCID 219302—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductOxane-4-carboxamideHCID 1319720346.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 0° C. solution of tetrahydro-2H-pyran-4-carboxylic acid (0.5 g, 3.84 mmol) in MeCN (15 mL) was treated with EDC (0.884 g, 4.61 mmol) and HOBT (0.706 g, 4.61 mmol) under an argon atmosphere and stirred at 0° C. for 1 h. Ammonium hydroxide (˜15M, 0.512 mL, 7.68 mmol) was added slowly and the mixture was warmed to RT and stirred overnight. The mixture was treated with water, saturated with solid NaCl and the aqueous layer was extracted with THF (2×). The combined organics were washed with brine, dried over Na2SO4 and concentrated to afford tetrahydro-2H-pyran-4-carboxamide (0.23 g, 46%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 7.20 (s, 1H), 6.73 (s, 1H), 3.82-3.81 (m, 2H), 3.30-3.21 (m, 2H), 2.30-2.27 (m, 1H), 1.60-1.46 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382228B2
Source datasetuspto-grants-2016_07
ORD IDord-26597227013d4270a58f748012e5294f
Source noteuspto-grants-2016_07