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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251289Generated: November 2, 2026

1-Decanol → L-lactide epsilon-caprolactone

https://huagongshe.com/reaction/1251289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-DecanolHCID 8174—
Reactant2-ethylhexanoic acid tin(II) saltHCID 9318—
Reactantepsilon-CAPROLACTONEHCID 10401—
ReactantLactide, L-HCID 107983—
ProductL-lactide epsilon-caprolactoneHCID 131710947—

Reaction Conditions

Temperature140 °C

Reaction Steps

In a typical reaction, l-lactide (6.67 moles, 960.5 g) and ε-caprolactone (0.35 moles, 39.9 g) were polymerized using decyl alcohol (7.02×10−3 moles, 1.11 g) as the initiator and stannous octoate (3.51×10−4 moles, 1.76 ml of 0.2 M solution in toluene) as the catalyst. The monomer to initiator ratio was 1,000 to 1; the monomer to catalyst ratio was 20,000 to 1. The reaction was carried out in a stainless steel resin kettle with a mechanical stirrer. The charge was dried under vacuum at 37° C. for 30 min. and 50° C. for 30 min. The monomer was then melted at 110° C. under positive argon pressure. Once melted, the charge was stirred at 32 rpm and heated to 140° C. After a short time at 140° C. the polymer solidified and could no longer be stirred. The polymerization was carried out for 48 hours at 140° C. followed by 16 hours at 120° C. The resulting polymer was characterized using GPC, DSC, viscosity, and carbon and proton NMR. The results for the three polymer lots made by this general method are summarized in Table I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342065B1
Source datasetuspto-grants-2002_01
ORD IDord-79101a221dbd463a9ce780ef3b190ae6
Source noteuspto-grants-2002_01