HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37438Generated: October 29, 2026
Carbon Dioxide → 4,4-Dimethyl-7-carboxythiochroman
https://huagongshe.com/reaction/37438
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 7-Bromo-4,4-dimethylthiochroman | HCID 22393099 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4,4-Dimethyl-7-carboxythiochroman | HCID 19935544 | — |
Reaction Steps
11 g of 7-bromo-3,4-dihydro-4,4-dimethyl-2H-1-benzothiopyran were dissolved in a mixture of 100 ml of ether and 10 ml of tetrahydrofuran and treated at -78° C. with 33 ml of a 1.6 molar solution of n-butyllithium in hexane. The reaction solution was held at -50° C. for 15 minutes, again cooled to -78° C. and gassed with carbon dioxide for 2 hours. Thereafter, the mixture was poured on to ice, acidified with 6N hydrochloric acid and extracted with ethyl acetate. The organic phases were washed with water, dried and evaporated. After recrystallization of the crude product from ethyl acetate/hexane, there were obtained 4.6 g of 3,4-dihydro-4,4-dimethyl-2H-1-benzothiopyran-7-carboxylic acid, melting point 202°-204° 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-81d03664d6ea416a9ade72f4f654a43d |
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| Source note | uspto-grants-1995_05 |
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