HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545485Generated: October 29, 2026
HCID 57443971, compound → HCID 57443968, compound
https://huagongshe.com/reaction/545485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57443971 | HCID 57443971 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57443968 | HCID 57443968 | — |
Reaction Steps
To a solution of benzo[b]thiophene-2,6-dicarboxylic acid 2-ethyl ester (6.40 g, 25.57 mmol) in 250 mL of anhydrous THF at 0° C. was slowly added BH3 (1.5M in THF, 80.0 mL, 120 mmol). The resulting mixture was allowed to stir at 0° C. for 30 min and at rt overnight. After cooling to 0° C., the reaction mixture was quenched with 1N HCl (30 mL). Additional 120 mL of water was added and THF was removed in vacuo. The solid formed was filtered and washed with 2×20 mL of water. After drying, 6-hydroxymethyl-benzo[b]thiophene-2-carboxylic acid ethyl ester was obtained as pale solid. 1H NMR (CDCl3, 200 MHz) δ 8.00 (s, 1H), 7.88-7.76 (m, 2H), 7.36 (d, J=9.4 Hz, 1H), 4.80 (s, 2H), 4.38 (q, J=7.0 Hz, 2H), 2.00 (brs, 1H), 1.39 (t, J=7.0 Hz, 3H). MS (EI): cal'd 237.0. (MH+), exp 237.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07935724B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-674d6a12b2c54e2ab18f069becf61119 |
|---|
| Source note | uspto-grants-2011_05 |
|---|