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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175051Generated: November 3, 2026

Water → Benzyl-(6-fluoroindan-1-yl)-amine

https://huagongshe.com/reaction/2175051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
ReactantBenzyl-(6-fluoroindan-1-ylidene)-amineHCID 90019076—
SolventEthanolHCID 702—
ProductBenzyl-(6-fluoroindan-1-yl)-amineHCID 9001938494.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve benzyl-(6-fluoroindan-1-ylidene)-amine (23.22 g, 97.03 mmol) in ethanol (1200 mL). Cool the mixture to 0° C. under nitrogen. Add sodium borohydride (11.01 g, 291.10 mmol) to the mixture. After one hour, add dichloromethane (150 mL) and water (150 mL). Stir for 14 hours under nitrogen and concentrate in vacuo to remove ethanol. Extract the residue with dichloromethane and saturated aqueous sodium chloride. Dry the resulting organics with magnesium sulfate, filter, and concentrate in vacuo to give the title compound as a red oil (22.12 g, 94%). MS (ES) m/z=242 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062050B2
Source datasetuspto-grants-2015_06
ORD IDord-ae1aeca5d76948d39fddeb53bcfb7b0c
Source noteuspto-grants-2015_06