Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 4,5,6,7-tetrahydro-5,5-dimethylbenzo[c]thiophene-1-carboxylate | HCID 57508883 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57437427 | HCID 57437427 | 81.3% |
Reaction Steps
To a solution of 5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid ethyl ester (715 mg, 3.0 mmol) in acetic acid (5 mL), bromine (480 mg, 3.0 mmol) is slowly added at rt. Upon completion of the addition, the mixture is heated to 50° C. and stirred for 4 h. The reaction is quenched by adding 1 N aq. NaOH and the mixture is extracted with DCM (3×50 mL). The organic extracts are dried (Na2SO4), filtered and evaporated to provide crude 3-bromo-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid ethyl ester (774 mg) as a brown oil; 1H NMR (CDCl3): δ 4.27 (q, J=7.6 Hz, 2H), 2.97 (t, J=7.0 Hz, 2H), 2.26 8 s, 2H), 1.51 (t, J=7.0 Hz, 2H), 1.33 8t, J=7.6 Hz, 3H), 0.95 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723378B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-530f4ef40f5d43cab3ef95beaffe9ba3 |
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| Source note | uspto-grants-2010_05 |
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