HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701213Generated: November 1, 2026
Water → N-(7-Hydroxy-4,5,6,7-tetrahydro-1-benzothiophen-4-yl)urea
https://huagongshe.com/reaction/1701213
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulbenox | HCID 65473 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(7-Hydroxy-4,5,6,7-tetrahydro-1-benzothiophen-4-yl)urea | HCID 20348930 | — |
Reaction Steps
In 2.5 liters of ethanol, 34.85 grams of (-)-4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-ylurea is stirred and 9.8 grams of NaBH4 is added. The mixture is stirred overnight at room temperature, 1400 ml. of water is added, and after stirring for 0.5 hour the ethanol is evaporated in vacuo. The mixture is cooled and 25-30 ml. of acetic acid is added until no more foaming occurs. The mixture is stirred for 0.75 hour, filtered to collect the first crop and this solid is washed with water and air dried. This solid is recrystallized from acetone and then from acetone/methanol to give 6.75 g. of isomer B of the title compound, m.p. 211°-213° C. (dec.), [α]D25.5 =-23.23° (c, 3.11 in methanol). This material contains 92% isomer B and 8% isomer A when assayed by high pressure liquid chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04191830 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-2a9d414efec94b42bc2ab2b66d1d0fe1 |
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| Source note | uspto-grants-1980_03 |
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