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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362855Generated: October 31, 2026

Ammonium Hydroxide → HCID 15491029, compound

https://huagongshe.com/reaction/362855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 23293589HCID 23293589—
SolventDichloromethaneHCID 6344—
ProductHCID 15491029HCID 1549102995.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 30% aqueous ammonium hydroxide (10 ml, 76 mmol, Mallinckrodt) was added to the solution of (E)-2-(6-fluoro-3,3-dimethyl-1-indanylidene)acetyl chloride (0.01363 mol) obtained from Example 41h diluted with dichloromethane (200 ml) and cooled to 0° C. The biphasic solution was stirred rapidly and allowed to warm to room temperature over 18 h. The reaction solution was concentrated by spin evaporation in vacuo, diluted with dichloromethane (200 ml), and washed with IN aqueous hydrochloric acid (McIntosh), a solution of 5% aqueous sodium bicarbonate (Mallinckrodt), dried with magnesium sulfate (Mallinckrodt), and concentrated by spin evaporation in vacuo. The residue was chromatographed on Silica Gel 60 using ethyl acetate-hexanes (1:1), and then ethyl acetate. Fractions containing (E)-2-(6-fluoro-3,3-dimethyl-1-indanylidene) acetamide were combined and concentrated by spin evaporation in vacuo. Recrystallization from dichloromethane-hexanes gave 2.85 g (95%) of (E)-2-(6fluoro-3,3-dimethyl-1-indanylidene)acetamide as a white crystalline solid, m.p., 167°-168° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872118
Source datasetuspto-grants-1999_02
ORD IDord-5b5566eddc7947c39714ee85536994ac
Source noteuspto-grants-1999_02