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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429587Generated: October 26, 2026

Retinoyl chloride → Retinamide

https://huagongshe.com/reaction/429587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRetinoyl chlorideHCID 10881705—
ReactantAzane;hydrateHCID 12896473—
SolventTetrahydrofuranHCID 8028—
ProductRetinamideHCID 537022199%

Reaction Steps

10 g (0.031 mole) of retinoic acid chloride as prepared according to the procedure described in Example 2 was added to the mixture of 300 ml of ammonia water (35%) and 100 ml of tetrahydrofuran and then stirred at room temperature for 20 hours. The reaction solution was distilled under reduced pressure and then concentrated. The residue was extracted with methylene chloride. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, filtered and then distilled under reduced pressure to obtain 9.43 g (Yield 99%) of the desired retinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316644B1
Source datasetuspto-grants-2001_11
ORD IDord-6572553c177743bea7be0af2dd8a8236
Source noteuspto-grants-2001_11