Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | epsilon-CAPROLACTONE | HCID 10401 | — |
| Catalyst | HCID 131716952 | HCID 131716952 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86744912 | HCID 86744912 | — |
Reaction Steps
The one-liter reactor described in Example 1 was charged with a 480 molecular weight poly(propylene oxide) triol initiator (78.9 g), zinc hexacyanocobaltate/zinc chloride/glyme/water catalyst (0.575 g, 1000 ppm), and tetrahydrofuran (60 mL). The load cell was charged with a mixture of ε-caprolactone (140 g) and propylene oxide (357 g). The reactor was purged several times with nitrogen, then pressurized to about 5 psi. The reactor contents were stirred and heated to 90° C. over a 1.5 hour period. An initial charge of 37 g of the ε-caprolactone/PO mixture was added to the reactor. A pressure drop was observed about 1 hour after addition of the initial charge, indicating that initiation of the catalyst had occurred. The remainder of the ε-caprolactone/PO mixture was added over about a 10-hour period. The product was heated for an additional 8 hours at 90° C. following addition of the monomer mixture, then cooled, drained from the reactor, and filtered through diatomaceous earth. Tetrahydrofuran was removed using a rotary evaporator. Residual ε-caprolactone was removed by passing the polymer product through a wiped-film evaporator under vacuum at 150° C. The triol product had a hydroxyl number of 51.0 mg KOH/g and a GPC number average molecular weight of 2980.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05032671 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-089c57043a6a413a8725066ee5f3c339 |
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| Source note | uspto-grants-1991_07 |
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