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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240807Generated: October 30, 2026

Bromine → HCID 57437427, compound

https://huagongshe.com/reaction/2240807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantEthyl 4,5,6,7-tetrahydro-5,5-dimethylbenzo[c]thiophene-1-carboxylateHCID 57508883—
SolventAcetic AcidHCID 176—
ProductHCID 57437427HCID 5743742781.3%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723378B2
Source datasetuspto-grants-2010_05
ORD IDord-530f4ef40f5d43cab3ef95beaffe9ba3
Source noteuspto-grants-2010_05