HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769201Generated: October 30, 2026
Hydrochloric Acid → 1-[4-(Hydroxymethyl)phenyl]-2-cyanoindole
https://huagongshe.com/reaction/1769201
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Carboxyphenyl)-2-cyanoindole | HCID 10400461 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 1-[4-(Hydroxymethyl)phenyl]-2-cyanoindole | HCID 10354639 | 56.1% |
Reaction Steps
2.8 g (0.0107 mol) of 1-(4-carboxyphenyl)-2-cyanoindole was dissolved in 100 ml tetrahydrofuran and cooled in an ice-bath. 1.5 ml (0.01 mol) of triethylamine was added, followed by the dropwise addition of 1.1 ml (0.01 mol) ethyl chloroformate. After stirring for 20 minutes the precipitate was removed by filtration and a solution of 1.2 g (0.1 mol) sodium borohydride in 60 ml tetrahydrofuran-water 3:1 was added dropwise to the filtrate. After stirring an additional 20 minutes, 5 ml of 10% hydrochloric acid was added, and the mixture extracted with ethyl acetate. The extract was dried over magnesium sulfate and evaporated to an oil. The oily material was chromatographed on silica gel, eluting with ethyl acetate-hexane 7:3 to give 1.5 g (0.006 mole) of 1-[4-(hydroxymethyl)phenyl]-2-cyanoindole as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380739 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-4d1be5bfb4f9499baf49b0807332aa50 |
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| Source note | uspto-grants-1995_01 |
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