HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274790Generated: October 25, 2026
Glycolic Acid → Hydroxyacetic acid--2-hydroxypropanoic acid (1/1)
https://huagongshe.com/reaction/1274790
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycolic Acid | HCID 757 | — |
| Reactant | Glycolide | HCID 65432 | — |
| Reactant | Lactide, L- | HCID 107983 | — |
| Reactant | Tetrakis(octanoate);tin(4+) | HCID 9961620 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Hydroxyacetic acid--2-hydroxypropanoic acid (1/1) | HCID 36797 | — |
Reaction Steps
A PFA-made cylinder was charged with 35.72 g (0.248 mol) of recrystallized L-(-)-lactide and 162.4 g (1.4 mol) of glycolide, and 17.0 ml of bis-2-methoxyethyl phthalate, 0.20 ml of a toluene solution of tin octanoate at a molar concentration of 0.33 and 0.0626 g of glycolic acid were added. After toluene was removed under high vacuum of 0.1 mmHg, and purging with nitrogen was conducted twice, the contents were heated at 180° C. for 40 minutes with stirring. The heating was further continued for 4 hours and 20 minutes to conduct polymerization. The resultant polymer was ground into fine particles having a particle size of about 3 mm or smaller. The fine particles were dried at about 25° C. for 48 hours under reduced pressure of about 0.1 kPa, thereby obtaining a glycolic acid/lactic acid copolymer [Polymer (P-C2)]. The same process was conducted repeatedly to prepare a necessary amount of Polymer (P-C2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06159416 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-2139a5c674ad4bca9690416f4bbabdfa |
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| Source note | uspto-grants-2000_12 |
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