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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617674Generated: October 27, 2026

Methyl Lactate → Behenyl Lactate

https://huagongshe.com/reaction/617674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl LactateHCID 11040—
ReactantBehenyl AlcoholHCID 12620—
ReactantSodium hydrideHCID 24758—
ProductBehenyl LactateHCID 54124846—

Reaction Conditions

Temperature160 °C

Reaction Steps

Behenyl Lactate was prepared by reacting methyl lactate (Aldrich Chemical Company, Inc. of Milwaukee, Wis.) with Lanette 22 (behenyl alcohol, 90%, Henkel Corp. of Ambler, Pa.) in a transesterification reaction according to the following method: 0.2 g sodium hydride (60% in mineral oil) was added to 32.6 grams Lanette 22 at 70° C. in a 3-neck 250 ml glass flask purged with nitrogen and inserted with overhead stirrer, Dean Stark trap, thermometer, and condenser. To this was slowly added 9.4 g of methyl lactate and the contents were slowly heated to 160° C. and held at that temperature for one hour. At this temperature over 2 ml of methanol was collected. The contents were heated to 200° C. with a nitrogen sweep to remove any volatile components. After approximately 15 minutes at 200° C. the contents were cooled. Upon cooling the product crystallized and had a melting point of approximately 57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05951993
Source datasetuspto-grants-1999_09
ORD IDord-8d4aeea8441b4cb58061d2abd2cd24f6
Source noteuspto-grants-1999_09