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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255293Generated: October 30, 2026

2,2-Diethoxyethylamine → HCID 58168483, compound

https://huagongshe.com/reaction/1255293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DiethoxyethylamineHCID 69524—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 58168483HCID 58168483—

Reaction Steps

Sodium triacetoxyborohydride (10.6 g) was added to a cooled (0° C.) solution of aminoacetaldehyde diethyl acetal (5.8 mL) and tetrahydro-4H-pyran-4-one (3.7 mL) in dichloromethane (100 mL). The reaction was stirred for 18 h, allowing the temperature to warm to ambient conditions. Water (100 mL) was added, followed by portionwise addition of sodium bicarbonate (16.8 g), causing effervescence. The mixture was stirred vigorously for 1 h, and then allowed to partition. The phases were then separated and the aqueous phase extracted with more dichloromethane (50 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo to afford the titled compound as a colourless oil. Yield 8.3 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455483B2
Source datasetuspto-grants-2013_06
ORD IDord-b3b7c9afb81f41beacc3cd9b5fbd5100
Source noteuspto-grants-2013_06