HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050980Generated: October 26, 2026
Carbon Dioxide → 4,4-Dimethyl-3,4-dihydro-2H-1-benzothiopyran-6-carboxylic acid
https://huagongshe.com/reaction/2050980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Bromo-4,4-dimethylthiochroman | HCID 9816554 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 4,4-Dimethyl-3,4-dihydro-2H-1-benzothiopyran-6-carboxylic acid | HCID 19834228 | — |
Reaction Steps
To a stirred solution of 5.14 g (0.02 mmol) of 4,4-dimethyl-6-bromothiochroman in 40 ml of dry ether at -78° C. was added dropwise 28.2 ml of 1.7M (0.048 mmol) tertbutyllithium in pentane. The mixture was stirred at -78° C. for 2.5 hours and then treated with an excess of solid carbon dioxide. The mixture was warmed to room temperature and treated with sufficient water to dissolve the solids. The aqueous layer was then separated, acidified with dilute sulfuric acid and extracted with three portions of ether. The ether extracts were combined and washed successively with water and saturated NaCl solution and then dried (MgSO4). The solution was filtered and the solvent removed in-vacuo and the residue recrystallized from ethyl acetate and hexane to give the title compound as a white solid. PMR (CDCl3): δ1.37 (6H, s), 1.97 (2H, m), 3.08 (2H, m), 7.17 (1H, d, J~8.0 Hz), 7.74 (1H dd, J~8.0, 1.9 Hz), 8.11 (1H, d, J~1.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05015658 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-5fde764441854b05a4abe694d8060279 |
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| Source note | uspto-grants-1991_05 |
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