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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372556Generated: October 31, 2026

Ethanol → HCID 53686665, compound

https://huagongshe.com/reaction/372556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 131711105HCID 131711105—
SolventWaterHCID 962—
ProductHCID 53686665HCID 5368666598.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

7.3 g of sodium borohydride was added over 30 minutes at 15° C to a solution of 7.3 g of the product of Step A in 7 3 ml of ethanol and 7.3 ml of water and the mixture was stirred for an hour at 20° C. The mixture was made alkaline with concentrated sodium hydroxide and the ethanol was evaporated. Water was added thereto and the mixture was extracted with methylene chloride. The organic phase was washed with water, dried and evaporated to dryness to obtain 6.2 g of 7-allylamino-5ξ-hydroxy-6,7,8,9-tetrahydro [5H] benzocycloheptene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091115
Source datasetuspto-grants-1978_05
ORD IDord-f3c7cedc3099432b9a0b00020ba93c40
Source noteuspto-grants-1978_05