HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773808Generated: October 26, 2026
1,2-Cyclohexanedione → Methyl 3-acetyl-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate
https://huagongshe.com/reaction/1773808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Cyclohexanedione | HCID 13006 | — |
| Reactant | MS-1254 | HCID 3761561 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-acetyl-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate | HCID 71014115 | 27.6% |
Reaction Steps
Add methyl 2-(2-oxopropylthio)acetate (35.4 g, 183.2 mmol) to a freshly prepared solution of solid sodium (8.78 g, 381.5 mmol) in dry MeOH (300 mL) at 0° C., followed by addition of a solution of cyclohexane-1,2-dione (20 g, 152.6 mmol) in MeOH (30 mL). Stir the mixture at 0° C. for 30 min and then at 50-60° C. for additional 1.5 hour. Remove the solvent under vacuum and dilute the residue with water (100 mL). Extract the aqueous mixture with ethyl acetate (100 mL×3). The combined organic layers are washed with brine, dried over anhydrous Na2SO4, and evaporated under vacuum. Purify the residue by a flash column on silica gel eluting with PE:EtOAc (50:1 to 30:1) to afford methyl 3-acetyl-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate as a white solid (10 g, 27.6%). MS (m/z): 239 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255111B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-6067ffdf329241b9bc27c9f8eec8d250 |
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| Source note | uspto-grants-2016_02 |
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