HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056750Generated: October 30, 2026
2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid → 2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)ethanol
https://huagongshe.com/reaction/2056750
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid | HCID 69307806 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)ethanol | HCID 69306515 | — |
Reaction Steps
(5-Chloro-1,3-dihydro-2-benzofuran-1-yl)acetic acid (1.91 g, 9.0 mmol) was dissolved in dry THF (8 mL) under nitrogen and cooled to 0° C. Borane-dimethylsulfide complex (0.155 mL, 1.64 mmol) was added by syringe. After 1 h the cooling bath was removed and the solution was stirred at room temperature for 2 h. The solution was partitioned between saturated aqueous sodium hydrogen carbonate and diethyl ether. The aqueous layer was further extracted with ether, and the combined organic layers washed with brine, dried (MgSO4), filtered and concentrated in vacuo. This yielded the title compound as a white solid (>98% ee by chiral HPLC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07335660B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-979dfce3043c4d37a2d9a222ef4b9e10 |
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| Source note | uspto-grants-2008_02 |
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