HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylene Glycol Monomethyl Ether → HCID 131728281, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylene Glycol Monomethyl Ether | HCID 8134 | — |
| Reactant | 2-ethylhexanoic acid tin(II) salt | HCID 9318 | — |
| Reactant | Lactide, L- | HCID 107983 | — |
| Reactant | D,D-Dilactide | HCID 5325924 | — |
| Reactant | HCID 131728281 | HCID 131728281 | — |
| Product | HCID 131728281 | HCID 131728281 | — |
| Product | HCID 131728282 | HCID 131728282 | — |
Reaction Steps
Ringopening polymerization of lactide (L-lactide for system (A) and D-lactide for system B, each 5 g) was carried out using 2-(2-methoxyethoxy)ethanol (MEE, 0.556 g) as an initiator, and stannous octoate (0.093 g) as the catalyst. The polymerization was carried out in the melt at 130° C. for four hours to yield MEE-L-lactic acid oligomer (A) and MEE-D-lactic acid oligomer (B). FIG. 1 shows the reaction scheme for the synthesis of dex-lactate (8), in which the DP is the degree of polymerization and DS is the degree of substitution (number of lactic acid oligomers per 100 glucopyranose units of dextran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776359B1 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-29aa9c7e73964c1c965d400d8b79f949 |
| Source note | uspto-grants-2010_08 |