HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548222Generated: October 29, 2026
HCID 57443971, compound → HCID 57443968, compound
https://huagongshe.com/reaction/548222
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 57443971 | HCID 57443971 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57443968 | HCID 57443968 | 87% |
Reaction Steps
A solution of benzo[b]thiophene-2,6-dicarboxylic acid 2-ethyl ester (1.6 g, 6.4 mmol) in anhydrous THF (40 mL, 25 vol) was cooled to 0° C. To this BH3 (1M in THF, 30 mL, 30.0 mmol) was added slowly. The reaction was allowed to warm to r.t. and stirred for 3 h. The solution was then cooled to 0° C. and quenched using 1N HCl (7.5 mL). The reaction mixture was concentrated under vacuum to remove all THF and the resulting solid isolated by filtration and dried under vacuum to give 6-hydroxymethyl-benzo[b]thiophene-2-carboxylic acid ethyl ester (1.3 g, 87%). LCMS m/z 237 [M++H]+, 1H NMR (300 MHz, DMSO), δ: 1.34 (3H, t J=6.9 Hz, CH3), 4.35 (2H, q J=7.1 Hz, CH2), 4.65 (2H, s, CH2), 6.53 (1H, br s, OH), 7.42 (1H, d J=9.4 Hz), 7.98 (3H, m, ArH), 8.18 (1H, s, ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07939666B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-d77b7acfa0364e198fdbf77bb8f80056 |
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| Source note | uspto-grants-2011_05 |
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