Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 2,2-Bis(bromomethyl)-1,3-propanediol | HCID 18692 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Product | HCID 19858279 | HCID 19858279 | 22.6% |
Reaction Steps
To 2,2-bis(bromomethyl)propane-1,3-diol (100 g) was added potassium bicarbonate (80 g) and dimethyl sulphate (170 g). The mixture was stirred and heated to 100° C. After about 30 minutes at this temperature the reaction became very vigorous (Care!). After a further 2 hours heating and stirring the mixture had become very viscous. The mixture was cooled, made slightly basic by the addition of sodium bicarbonate, and then extracted with chloroform (4×200 cm3). The chloroform extracts were combined and the solvent removed under reduced pressure to give the crude product. Repeated distillation under reduced pressure gave the pure product (25 g) as a colourless liquid (b.p. 65°-70° C. at 0.1 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04916214 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-8dd18062c5e64115acd6283d92d216cb |
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| Source note | uspto-grants-1990_04 |
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