HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37437Generated: October 29, 2026
Carbon Dioxide → HCID 19935542, compound
https://huagongshe.com/reaction/37437
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 7-Bromo-4,4-dimethylchroman | HCID 22393100 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19935542 | HCID 19935542 | — |
Reaction Steps
A solution of 14.2 g of 7-bromo-3,4-dihydro-4,4-dimethyl-2H-1-benzopyran and 1.1 g of 1,2-dibromoethane in 80 ml of tetrahydrofuran was added dropwise using a heatable ultrasonics bath, to a suspension, boiling under reflux, of 1.6 g of magnesium shavings in 20 ml of tetrahydrofuran. After heating under reflux for an additional 2 hours, the reaction mixture was cooled to 0° C. and a strong stream of carbon dioxide gas was conducted in (about 1 hour). Thereafter, the mixture was poured on to ice, acidified with 2N hydrochloric acid and extracted with ethyl acetate. The organic extracts were washed with water, dried and evaporated. After recrystallization from ethyl acetate/hexane, there were obtained 5.3 g of 3,4-dihydro-4,4-dimethyl-2H-1-benzopyran-7-carboxylic acid, melting point 173°-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420273 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-fef4d12188df48b4b48a01b0d5a3505e |
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| Source note | uspto-grants-1995_05 |
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